130265775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31204352-C-G

130265903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31204451-C-T

130265928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31204476-C-T

130265940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31204488-C-T

130265946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31204497-C-T

http://identifiers.org/hco/9/GRCh38#130266019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31204570-C-A

130266094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31204645-C-T

http://identifiers.org/hco/9/GRCh38#130266142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31204693-C-A

130266142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31204693-C-T

130266195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31204740-T-C

http://identifiers.org/hco/9/GRCh38#130266197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31204742-A-C

130266279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31204809-G-A

130266279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31204809-G-C

130266279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31204809-G-T

130266321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31204854-C-T

130266427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31204963-T-C

130266427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31204963-T-G

130266431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31204967-C-G

130266966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31205367-G-A

130266966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31205367-G-C

130266966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31205367-G-T

130267127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31205509-A-G

130267187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31205572-C-T

130267337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31205773-T-C

http://identifiers.org/hco/9/GRCh38#130267559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31205903-C-A

130267650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31205961-C-T

130267743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31206024-C-T

130267787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31206067-G-A

130267841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31206095-G-A

130267946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31206184-C-T

130268051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31206278-G-A

130268108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31206321-G-A

130268119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31206332-T-C

130268121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31206334-G-C

http://identifiers.org/hco/9/GRCh38#130268157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31206367-C-A

130269114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31208573-C-T

130270170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31209798-A-G

130270186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31209814-A-G

130270225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31209851-A-G

130270225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31209851-A-T

130270243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31209871-G-T

130270503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31210101-G-T

http://identifiers.org/hco/9/GRCh38#130277057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31219637-A-C

130277057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31219637-A-G

130277058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31219638-T-C

130277467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31220008-T-A

130277469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31220010-G-A

130284628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31223892-G-A

130284628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31223892-G-T

130284679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31223943-C-T

130284726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31223987-T-C

130285149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31225417-G-A

http://identifiers.org/hco/9/GRCh38#130285205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31225473-C-A

130285205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31225473-C-T

130285223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31225491-C-G

130285223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31225491-C-T

130285286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31225554-G-A

130285286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31225554-G-T

130285354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31225617-C-G

130285354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31225617-C-T

130285549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31225742-G-A

130285568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31225760-G-A

130285568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31225760-G-T

http://identifiers.org/hco/9/GRCh38#130285577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31225769-C-A

130285580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31225772-C-T

130285684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31225903-G-A

130285937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226336-A-G

130285971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226369-C-T

130286208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31226539-G-T

130286256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31226587-C-T

130286354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226661-G-A

130286354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226661-G-C

130286354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226661-G-T

130286379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226684-T-A

130286379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226684-T-C

http://identifiers.org/hco/9/GRCh38#130286386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31226691-C-A

130286386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226691-C-G

130286489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226781-C-T

130286502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226796-A-G

130286595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226865-G-A

130286595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31226865-G-C

130286816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31227005-G-A

130287048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31227163-C-T

130287097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31227212-T-G

130287180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31227313-A-G

130287278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31227387-G-T

130287505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31227514-C-T

130287738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31227634-C-G

130287776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31227669-G-C

130288273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31228060-T-G

130288390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31228137-A-G

130288550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31228266-C-T

130288648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31228344-G-A

130288808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31228486-C-T

130288995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31228821-C-T

130289021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31228990-G-T

130289378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31229329-C-G

130289512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31229466-C-G

130289816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31229769-G-A

130289816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31229769-G-T

130289981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31229897-G-A

130289981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31229897-G-T

130290095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230013-G-C

130290141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230056-C-T

130290176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230089-C-G

130290176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230089-C-T

130290305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230252-G-A

130290540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230472-G-A

130290540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230472-G-C

130290541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230473-G-T

130290558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230490-T-C

130290655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230560-A-G

130290753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230659-A-T

130290807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230695-G-A

130290932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230771-G-T

130290947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230786-G-A

http://identifiers.org/hco/9/GRCh38#130290957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31230796-C-A

130290967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230806-A-G

130290985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230824-G-T

130291009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31230848-C-T

130294607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31232786-C-T

130294610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31232789-G-A

130294704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31232865-G-A

130294767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31232924-T-C

130294800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31232958-A-G

130294804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31232982-G-T

130294823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31233037-T-C

http://identifiers.org/hco/9/GRCh38#130294825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31233039-C-A

130294825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31233039-C-T

130294842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31233055-T-A

130294992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31233205-G-A

http://identifiers.org/hco/9/GRCh38#130295064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31233274-C-A

130295064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31233274-C-G

130295064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31233274-C-T

130295552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31233909-T-A

130295552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31233909-T-C

130295647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31234005-G-T

http://identifiers.org/hco/9/GRCh38#130295649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31234007-C-A

130296547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31234350-A-G

130296736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31234543-C-T

130296851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31234632-G-T

130296912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31234693-G-T

130297041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31234751-C-T

130297064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31234769-G-A

130298814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31236302-G-C

130298814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31236302-G-T

130298903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31236390-G-T

130299056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31236505-G-A

130299056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31236505-G-C

130299056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31236505-G-T

130299134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31236583-G-A

130299134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31236583-G-T

130299182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31236631-C-T

130299282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31236731-G-A

130299282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31236731-G-T

130299618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31236969-C-T

130299770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237088-T-C

130299831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237117-T-C

130299832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237118-C-T

130299876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237144-C-T

http://identifiers.org/hco/9/GRCh38#130299912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31237182-C-A

130300147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237327-G-A

130300147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237327-G-C

130300152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237332-C-T

130300258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237427-C-T

http://identifiers.org/hco/9/GRCh38#130300630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31237711-A-C

130300748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237750-C-T

130300755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237756-G-A

130300921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31237903-C-T

130301365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31238311-T-C

130301368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31238314-C-G

130301478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31238423-C-T

130301591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31238538-C-T

130301675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31238613-G-A

http://identifiers.org/hco/9/GRCh38#130301859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31238790-C-A

130301973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31238901-G-A

130302728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31239829-G-A

130302728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31239829-G-T

http://identifiers.org/hco/9/GRCh38#130302781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31239906-C-A

http://identifiers.org/hco/9/GRCh38#130302782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31239907-C-A

http://identifiers.org/hco/9/GRCh38#130302786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31239911-A-C

130302786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31239911-A-G

130302891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31240024-T-C

http://identifiers.org/hco/9/GRCh38#130302910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31240043-C-A

130303128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240236-G-A

130303136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240244-T-C

130303243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240317-A-G

130303358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240403-G-A

130303358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240403-G-C

http://identifiers.org/hco/9/GRCh38#130303373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31240418-C-A

http://identifiers.org/hco/9/GRCh38#130303394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31240439-C-A

130303406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240450-G-A

130303406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240450-G-T

130303407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240451-G-A

130303407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240451-G-C

130303407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240451-G-T

130303422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240467-A-G

130303493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31240537-G-A

130303493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31240537-G-T

130303560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31240604-G-A

130303560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31240604-G-T

130303590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31240634-G-A

130303590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31240634-G-T

130303631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240671-A-T

130303633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240673-G-C

130303633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240673-G-T

130303673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240705-G-A

130303673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240705-G-T

http://identifiers.org/hco/9/GRCh38#130303681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31240713-C-A

130303844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240793-C-T

130303909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240812-G-A

130303915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240816-G-A

130303940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240843-C-T

130303959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240862-C-T

130303960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240863-G-A

130303960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31240863-G-C

130304323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31242303-A-T

130304418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31242364-T-G

130304555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31242499-T-C

130304857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31242748-G-A

130304908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31242799-C-T

130304910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31242801-G-A

130304913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31242804-G-C

130304974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31242865-A-G

http://identifiers.org/hco/9/GRCh38#130305066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31242957-A-C

130305066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31242957-A-T

130305538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31243263-G-A

130305555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31243279-C-T

130305752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31243449-A-G

130305956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31243589-C-T

130306240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31243839-G-A

130306240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31243839-G-C

130306283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31243879-G-T

http://identifiers.org/hco/9/GRCh38#130306288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31243884-C-A

130306288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31243884-C-T

130306289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31243885-A-G

130306344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31243938-T-A

130306388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31243976-G-A

http://identifiers.org/hco/9/GRCh38#130306389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31243977-C-A

130306389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31243977-C-T

http://identifiers.org/hco/9/GRCh38#130306682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31244063-C-A

130306682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244063-C-T

130306800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244167-C-T

130306801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244168-A-G

130306803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31244170-G-T

http://identifiers.org/hco/9/GRCh38#130306925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31244292-C-A

130306978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244333-T-C

http://identifiers.org/hco/9/GRCh38#130306996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31244349-C-A

130306996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244349-C-G

130306996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244349-C-T

http://identifiers.org/hco/9/GRCh38#130307007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31244360-C-A

130307052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244397-G-A

130307052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244397-G-T

http://identifiers.org/hco/9/GRCh38#130307318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31244515-C-A

http://identifiers.org/hco/9/GRCh38#130307326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31244520-C-A

130307326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244520-C-T

http://identifiers.org/hco/9/GRCh38#130307328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31244522-C-A

130307328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244522-C-G

130307343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244538-A-G

130307345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244540-G-T

130307352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244547-T-C

130307717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31244878-G-A

130309778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31246123-A-G

130309803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31246148-G-A

130309803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31246148-G-T

http://identifiers.org/hco/9/GRCh38#130309866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31246194-A-C

http://identifiers.org/hco/9/GRCh38#130309899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31246223-C-A

130309952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31246276-T-C

130309952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31246276-T-G

http://identifiers.org/hco/9/GRCh38#130310208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31246491-A-C

130310208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31246491-A-G

130313186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31247433-C-T

130313593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31247903-T-C

130316739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31249150-C-T

130316826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31249244-G-C

130316930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31249340-G-C

130316973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31249385-G-A

130317130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31249507-A-G

130317311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31249645-T-A

130317311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31249645-T-C

130317396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31249722-T-C

http://identifiers.org/hco/9/GRCh38#130319460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31250855-C-A

130319460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31250855-C-T

130319466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31250865-G-A

130319517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31250915-G-A

130319517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31250915-G-T

130319527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31250925-G-A

130319527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31250925-G-C

130319527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31250925-G-T

130319568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31250966-G-A

130319568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31250966-G-T

http://identifiers.org/hco/9/GRCh38#130319604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31251002-C-A

130319604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31251002-C-T

130319607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31251005-C-T

http://identifiers.org/hco/9/GRCh38#130319621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31251019-C-A

130319621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31251019-C-G

130319625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31251023-G-A

130319719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251105-G-A

130319719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251105-G-C

130319719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251105-G-T

130319729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251115-G-A

130319729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251115-G-T

130320067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251625-C-T

http://identifiers.org/hco/9/GRCh38#130320210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31251706-C-A

130320210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251706-C-G

130320218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251714-T-G

130320282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251758-G-T

130320316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251776-G-A

130320316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251776-G-T

130320366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31251819-A-G

130320378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31251831-C-T

130320381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31251834-A-G

130320408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31251861-T-C

http://identifiers.org/hco/9/GRCh38#130320438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31251891-C-A

130320438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31251891-C-T

130320526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251962-G-A

130320526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31251962-G-T

130320570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31252000-A-G

130320633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31252047-T-A

130320633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31252047-T-C

130320697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31252111-G-T

130320698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31252112-A-G

http://identifiers.org/hco/9/GRCh38#130320831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31252225-C-A

130320831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31252225-C-T

130320832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31252226-G-A

130320832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31252226-G-T

http://identifiers.org/hco/9/GRCh38#130320867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31252261-C-A

130320867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous_variant, undefined
orthologous variants: 31252261-C-T

130320920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31252314-T-C

130320963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31252350-T-C

130321619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254113-G-A

130321707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254188-G-A

130321707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254188-G-C

130321707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254188-G-T

130321713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254194-T-A

130321803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31254245-G-A

130321803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31254245-G-T

http://identifiers.org/hco/9/GRCh38#130321822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31254264-C-A

130321822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31254264-C-T

130321864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31254306-G-T

http://identifiers.org/hco/9/GRCh38#130321897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31254339-C-A

130321945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254387-T-C

130321960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254400-T-C

130321964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254404-G-A

130321964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254404-G-C

130321964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254404-G-T

130322049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254446-A-G

130322177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31254543-C-T

130325473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31258845-G-T

130325520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31258893-G-A

130325520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31258893-G-T

130325580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31258948-G-T

130325629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31258997-T-C

http://identifiers.org/hco/9/GRCh38#130325632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31259000-C-A

130325632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31259000-C-T

130325732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259109-G-T

130325734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259111-T-C

130325782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259158-C-T

130325796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259171-G-T

130325800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259175-C-T

130325820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31259195-G-A

http://identifiers.org/hco/9/GRCh38#130325891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31259263-C-A

130325995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259363-G-A

130326044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259412-G-A

130326044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259412-G-T

130326238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259596-G-C

130326304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259644-A-G

130326525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259868-A-G

130326573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31259911-T-G

130326670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260026-T-G

130326753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260158-C-T

130326754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260159-G-A

130326766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260197-C-G

130326766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260197-C-T

130326767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260198-G-A

130326767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260198-G-C

130326787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260238-A-G

http://identifiers.org/hco/9/GRCh38#130327181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31260691-C-A

130327182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260692-T-A

130327182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260692-T-C

130327214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260722-G-A

130327226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31260734-G-A

130327226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31260734-G-C

130327226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31260734-G-T

http://identifiers.org/hco/9/GRCh38#130327238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31260746-C-A

130327238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260746-C-G

130327351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31260834-G-T

130327429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31260912-G-A

130327498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31260976-A-G

130327561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31261039-T-C

130327562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31261040-T-C

130327562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31261040-T-G

http://identifiers.org/hco/9/GRCh38#130327596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31261066-C-A

130327978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31261409-T-C

130328047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31261476-G-T

130328705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31262065-G-A

130328705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31262065-G-C

130328785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31262129-G-T

130328811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31262155-G-A

130328871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31262220-G-A

http://identifiers.org/hco/9/GRCh38#130330306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31263508-C-A

130330306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31263508-C-T

130330348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31263557-C-T

130330351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31263560-C-T

130330542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31263766-C-T

http://identifiers.org/hco/9/GRCh38#130330543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31263767-A-C

130330593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31263878-G-C

http://identifiers.org/hco/9/GRCh38#130330650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31263932-C-A

http://identifiers.org/hco/9/GRCh38#130331565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31264468-C-A

130331601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31264490-C-T

http://identifiers.org/hco/9/GRCh38#130331624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31264506-C-A

130331768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31264641-A-T

130332148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31264917-A-T

130332188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31264957-G-A

130332352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31265070-C-T

130332531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31265249-C-T

130332579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31265266-C-T

130332624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31265296-C-T

130332843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31265493-G-A

130332878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31265552-G-A

130332984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31265649-T-G

130333012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31265687-T-C

130333012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31265687-T-G

130333185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31265866-G-A

http://identifiers.org/hco/9/GRCh38#130333449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31266248-C-A

130333633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31266430-T-C

130333634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31266431-T-C

130333744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31266508-C-G

130333744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31266508-C-T

130334230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31266907-A-G

130334265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31266936-G-A

130334410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267040-C-G

130334420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267050-A-G

130334422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267052-T-C

130334451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267086-T-C

130334452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267087-A-G

130336936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267452-G-T

130336953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267469-G-T

130337034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267539-C-T

130337035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267540-C-T

130337052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267557-C-G

130337200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267678-G-A

130337302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267754-C-G

130337580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31267981-G-A

130337745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268097-G-A

130337757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268111-G-A

130337757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268111-G-T

130337822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268183-A-G

130337846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268207-T-C

130337846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268207-T-G

http://identifiers.org/hco/9/GRCh38#130337868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31268227-C-A

130337868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268227-C-T

130337934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31268293-G-A

130337934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31268293-G-T

http://identifiers.org/hco/9/GRCh38#130337981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31268340-C-A

130337981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31268340-C-T

http://identifiers.org/hco/9/GRCh38#130337983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31268342-C-A

130337983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31268342-C-T

130338001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31268360-G-A

130338001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31268360-G-T

http://identifiers.org/hco/9/GRCh38#130338005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#31268364-C-A

130338005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31268364-C-T

130338006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31268365-G-A

130338006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31268365-G-T

http://identifiers.org/hco/9/GRCh38#130338056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31268412-C-A

130338056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31268412-C-T

130338060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant
orthologous variants: 31268416-C-T

http://identifiers.org/hco/9/GRCh38#130338065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31268421-C-A

130338065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31268421-C-T

130338601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31268710-C-T

130338619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268728-G-A

130338619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268728-G-T

130338650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268746-G-C

130338650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268746-G-T

130338653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31268749-C-T

130340917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270030-C-G

130340941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270057-A-G

http://identifiers.org/hco/9/GRCh38#130341003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31270133-C-A

130341025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270155-G-T

130341034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270164-G-C

130341034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270164-G-T

130341040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270170-G-A

130341040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270170-G-T

130341050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270180-G-T

130341059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270189-G-T

130341072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270200-G-A

130341072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270200-G-T

130341127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31270256-G-A

130341127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31270256-G-T

130341159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31270288-G-T

130341245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31270374-C-T

http://identifiers.org/hco/9/GRCh38#130341265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31270394-C-A

130341265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31270394-C-T

http://identifiers.org/hco/9/GRCh38#130341285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31270414-C-A

130341420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270528-T-C

130341824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270800-C-T

130342159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270933-G-C

130342246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270971-A-G

http://identifiers.org/hco/9/GRCh38#130342252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31270977-C-A

130342252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31270977-C-T

130342296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271006-G-A

130342296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271006-G-T

130342316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271019-G-A

130342316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271019-G-T

130342343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31271048-C-T

http://identifiers.org/hco/9/GRCh38#130342402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31271106-C-A

130342402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31271106-C-T

130342411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31271115-T-C

130342423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31271127-G-A

130342423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31271127-G-T

130342452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271156-G-A

130342452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271156-G-T

130342476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271180-G-A

130342476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271180-G-T

http://identifiers.org/hco/9/GRCh38#130342478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31271182-C-A

130342478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271182-C-T

130343572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31271386-G-A

130343572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31271386-G-T

130343666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271496-C-T

130343688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271518-G-A

130346680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271889-G-A

130346683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31271892-C-T

130346813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31272000-C-T

130346938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31272093-A-T

130347032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31272208-G-A

130347032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31272208-G-C

130347032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31272208-G-T

130347199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31272372-G-A

130347199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31272372-G-T

130347223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31272396-G-A

130347223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31272396-G-T

130347239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31272412-A-G

130347239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31272412-A-T

130347250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31272423-A-G

http://identifiers.org/hco/9/GRCh38#130347410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31272561-C-A

130347410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31272561-C-T

http://identifiers.org/hco/9/GRCh38#130347431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31272582-C-A

130347431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31272582-C-T

http://identifiers.org/hco/9/GRCh38#130347615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31272707-A-C

130347766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31272843-A-T

http://identifiers.org/hco/9/GRCh38#130347894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31273044-C-A

130347894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273044-C-T

http://identifiers.org/hco/9/GRCh38#130347936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31273071-C-A

130347936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273071-C-G

130347936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273071-C-T

130347943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273078-T-C

130348163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273267-G-T

130348360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273449-G-A

http://identifiers.org/hco/9/GRCh38#130348432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31273524-C-A

130348432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273524-C-T

130348434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273526-G-T

130348461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273571-G-A

130348461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273571-G-T

130348475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273585-A-G

130348475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273585-A-T

130348499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273609-T-A

130348516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273631-G-T

130348572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31273689-G-A

130348572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31273689-G-T

130348672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31273789-G-A

130348694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273804-T-G

130348705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273815-T-G

130348814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273915-G-A

130348814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273915-G-T

130348852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273952-G-C

130348852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273952-G-T

130348872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273971-T-C

http://identifiers.org/hco/9/GRCh38#130348878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31273977-C-A

130348878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273977-C-T

130348891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31273986-G-T

130348969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274037-G-A

130349006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31274074-G-A

130349100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31274168-C-G

130349100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31274168-C-T

130349259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274522-A-G

http://identifiers.org/hco/9/GRCh38#130349267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31274530-C-A

130349267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274530-C-T

130349276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274542-T-C

http://identifiers.org/hco/9/GRCh38#130349279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31274545-C-A

130349299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274607-G-A

130349299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274607-G-T

130349390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274732-T-C

130349390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274732-T-G

130349408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274747-G-T

http://identifiers.org/hco/9/GRCh38#130349442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31274770-C-A

130349442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274770-C-T

130349450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274778-G-A

130349450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274778-G-T

130349477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274792-G-T

130349522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274836-C-G

130349522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274836-C-T

130349566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31274880-G-A

130349566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31274880-G-C

130349566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31274880-G-T

130349580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31274894-A-T

130349603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31274917-A-T

http://identifiers.org/hco/9/GRCh38#130349633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31274947-C-A

130349633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31274947-C-T

130349646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31274960-G-A

130349646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31274960-G-T

130349685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274993-G-A

130349685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31274993-G-T

130349700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275007-T-C

http://identifiers.org/hco/9/GRCh38#130349773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31275052-A-C

130349773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275052-A-G

130349786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275065-G-A

130349786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275065-G-T

130349796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275074-G-A

130349796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275074-G-T

130349844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275119-C-T

http://identifiers.org/hco/9/GRCh38#130351377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31275128-C-A

130351377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275128-C-T

130351378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275129-A-G

130351426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31275165-T-A

130351426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31275165-T-C

130351571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31275310-G-A

130351571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31275310-G-T

130351619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275349-A-G

http://identifiers.org/hco/9/GRCh38#130351637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31275367-C-A

130351637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275367-C-G

130351637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275367-C-T

130351673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275406-T-C

130351673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275406-T-G

130351697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31275414-G-T

130352731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276450-C-T

130352761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276480-A-G

130352857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276570-T-G

http://identifiers.org/hco/9/GRCh38#130352988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31276684-A-C

130353057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31276753-G-A

130353057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31276753-G-T

http://identifiers.org/hco/9/GRCh38#130353093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31276789-C-A

130353093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31276789-C-T

130353124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31276820-A-T

130353145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31276841-A-G

http://identifiers.org/hco/9/GRCh38#130353174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31276870-C-A

130353174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31276870-C-T

130353225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276916-G-A

130353233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276924-G-A

130353233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276924-G-T

130353293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276986-G-A

130353293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276986-G-T

130353303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276994-T-A

130353303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276994-T-C

130353303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31276994-T-G

130353435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31277105-C-T

http://identifiers.org/hco/9/GRCh38#130353674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31277280-C-A

http://identifiers.org/hco/9/GRCh38#130353837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31277412-A-C

130353979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31277523-C-G

130353979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31277523-C-T

130354171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31277696-T-C

130354605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278056-C-T

130354649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278090-A-G

130354733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278150-T-C

130354816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31278232-G-A

130354869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31278285-C-G

130354891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31278307-C-G

130355022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31278435-G-A

130355022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31278435-G-T

130355047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278460-G-A

http://identifiers.org/hco/9/GRCh38#130355103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31278494-C-A

130355103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278494-C-T

130355110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278501-C-T

http://identifiers.org/hco/9/GRCh38#130355175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31278556-C-A

130355175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278556-C-G

130355175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278556-C-T

130355215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278593-C-T

130355408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278748-T-C

http://identifiers.org/hco/9/GRCh38#130355584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31278887-C-A

130355714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31278987-T-C

130355738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31279007-G-A

130355847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31279116-A-G

http://identifiers.org/hco/9/GRCh38#130356082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31279261-C-A

130356082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31279261-C-T

130356083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31279262-C-G

http://identifiers.org/hco/9/GRCh38#130356138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31279317-C-A

130356138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31279317-C-T

130356241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31279420-G-T

130356298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279478-A-G

130356298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279478-A-T

130356316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279494-G-T

130356355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279535-G-T

130356356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279536-T-A

http://identifiers.org/hco/9/GRCh38#130356406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31279576-C-A

130356406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279576-C-T

130356407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279577-G-A

130356407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279577-G-T

130356428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279599-G-A

130356437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279608-T-A

130356577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279710-T-C

130356602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279723-C-T

130356768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279864-G-A

http://identifiers.org/hco/9/GRCh38#130356893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31279987-A-C

130356893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279987-A-G

130356893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31279987-A-T

130356914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280008-G-A

130357234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280345-G-A

130357235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280346-T-G

130357246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280357-A-G

130357273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280380-G-C

130357276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280383-G-A

130357278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280385-G-A

130357285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280392-G-A

130357288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280395-G-T

130357322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280429-G-A

130357323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280430-T-G

130357345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280451-A-G

130357597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280721-G-A

130357597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280721-G-T

http://identifiers.org/hco/9/GRCh38#130357727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31280844-C-A

130357763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280880-G-A

130357763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280880-G-T

130357765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280882-G-A

130357765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280882-G-T

130357793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31280910-T-C

130357856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31280974-T-C

130357913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31281031-G-A

130357913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31281031-G-T

130357956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31281074-G-A

130358013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31281130-G-A

130358096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31281175-A-G

http://identifiers.org/hco/9/GRCh38#130358117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31281197-C-A

130358117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31281197-C-G

http://identifiers.org/hco/9/GRCh38#130358227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31281249-C-A

http://identifiers.org/hco/9/GRCh38#130358228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31281250-C-A

130358350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31281381-G-A

130358392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 31281444-T-G

130358597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31281622-A-G

130358620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31281645-A-G

130359249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282072-G-A

130359249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282072-G-T

130359286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282109-T-C

http://identifiers.org/hco/9/GRCh38#130359288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31282111-C-A

130359288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282111-C-T

130359294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282117-T-A

130359352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31282175-A-G

130359355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31282178-C-T

130359404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31282227-G-A

130359430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282253-T-C

130359970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282661-G-A

130359970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282661-G-C

130359970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282661-G-T

130360033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282717-G-T

130360110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282787-G-A

130360149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282826-T-C

130360221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282891-G-A

130360221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31282891-G-T

http://identifiers.org/hco/9/GRCh38#130360423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31282969-C-A

130360423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31282969-C-T

130360567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31283113-A-G

130360567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31283113-A-T

130360644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31283228-G-A

130360644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31283228-G-T

130360663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31283250-G-A

http://identifiers.org/hco/9/GRCh38#130360667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31283254-A-C

130360667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31283254-A-G

http://identifiers.org/hco/9/GRCh38#130360713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31283306-C-A

130360713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31283306-C-T

130360808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31283420-T-A

http://identifiers.org/hco/9/GRCh38#130361748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31284479-C-A

130361865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284572-A-T

130361891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284594-G-A

130361891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284594-G-T

http://identifiers.org/hco/9/GRCh38#130361950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31284651-C-A

130361950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284651-C-T

http://identifiers.org/hco/9/GRCh38#130361965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31284654-C-A

130361965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284654-C-T

http://identifiers.org/hco/9/GRCh38#130361994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31284687-C-A

130361994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284687-C-T

130362025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31284718-C-T

130362035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31284728-G-A

130362035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31284728-G-T

130362036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31284729-C-T

130362039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31284732-G-A

http://identifiers.org/hco/9/GRCh38#130362090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31284783-C-A

130362090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31284783-C-T

http://identifiers.org/hco/9/GRCh38#130362152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31284845-C-A

http://identifiers.org/hco/9/GRCh38#130362192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31284885-C-A

130362192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284885-C-T

130362201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284894-T-A

130362201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284894-T-C

130362229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284922-G-A

130362229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284922-G-T

130362234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31284927-G-A

130362722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31285897-C-T

130362776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31285954-G-A

130362776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31285954-G-T

http://identifiers.org/hco/9/GRCh38#130362777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31285955-C-A

130362777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31285955-C-T

130362781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31285959-G-A

http://identifiers.org/hco/9/GRCh38#130362782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31285960-C-A

130362782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31285960-C-T

http://identifiers.org/hco/9/GRCh38#130362881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31286047-C-A

130362881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31286047-C-G

130362881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31286047-C-T

130362975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31286141-G-A

130362975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31286141-G-T

130363035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286195-G-A

130363035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286195-G-T

http://identifiers.org/hco/9/GRCh38#130363056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31286235-C-A

130363056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286235-C-T

http://identifiers.org/hco/9/GRCh38#130363057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31286236-C-A

130363057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286236-C-T

130364652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286601-G-A

130364652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286601-G-T

130364661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286610-T-C

130364683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286625-G-T

130364696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286638-T-C

http://identifiers.org/hco/9/GRCh38#130364698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31286640-C-A

http://identifiers.org/hco/9/GRCh38#130364707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31286649-C-A

130364842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: stop gained
orthologous variants: 31286784-G-T

130364914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286873-G-A

130364914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286873-G-C

130364914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286873-G-T

130364956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286901-G-A

130364996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31286937-G-T

130365150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287050-C-T

130365271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287180-A-G

130365450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287339-C-T

130365515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287398-G-A

130365515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287398-G-T

http://identifiers.org/hco/9/GRCh38#130365533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31287411-C-A

130365533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287411-C-T

http://identifiers.org/hco/9/GRCh38#130365544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31287422-C-A

130365544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287422-C-T

http://identifiers.org/hco/9/GRCh38#130365660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31287517-C-A

130365660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31287517-C-T

http://identifiers.org/hco/9/GRCh38#130365666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#31287523-C-A

130365666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31287523-C-T

130365755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287609-G-A

130365755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287609-G-T

130365774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287623-T-C

http://identifiers.org/hco/9/GRCh38#130365781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31287630-C-A

130365781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287630-C-T

130365798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287646-T-C

130365802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287650-G-A

130365802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287650-G-T

http://identifiers.org/hco/9/GRCh38#130366019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31287844-C-A

130366019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287844-C-T

http://identifiers.org/hco/9/GRCh38#130366020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31287845-C-A

130366020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31287845-C-T

130368153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31288796-A-G

http://identifiers.org/hco/9/GRCh38#130368160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31288803-C-A

130368160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31288803-C-T

130368167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31288810-G-A

130368167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31288810-G-T

130368196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31288827-G-A

130368196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31288827-G-T

http://identifiers.org/hco/9/GRCh38#130368200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31288831-A-C

http://identifiers.org/hco/9/GRCh38#130368283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31288900-C-A

130368283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31288900-C-T

130368319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31288936-G-A

130368319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31288936-G-T

130368325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31288942-G-C

130368346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31288963-A-G

130368373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31288990-A-G

130368373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31288990-A-T

130368400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31289017-G-A

130368400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31289017-G-T

130368523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31289118-G-T

130368578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31289150-T-A

130368581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31289153-G-A

130368581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31289153-G-T

130368926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31289439-G-A

130369034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31289519-C-G

130369046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31289522-G-A

130369052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, undefined
orthologous variants: 31289528-A-G

http://identifiers.org/hco/9/GRCh38#130369066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31289535-A-C

130369239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31289687-A-T

130369308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31289743-G-T

http://identifiers.org/hco/9/GRCh38#130369426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31289867-A-C

130369426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31289867-A-G

130369496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31289956-G-T

130369508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31289968-A-G

130369673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31290134-G-A

130369673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31290134-G-T

http://identifiers.org/hco/9/GRCh38#130369859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31290320-C-A

130369859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31290320-C-T

130370000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31290434-G-A

130370000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31290434-G-T

130370728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31291380-G-C

130370831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31291494-T-C

130370873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31291539-G-A

130370873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31291539-G-T

130370914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31291564-G-A

130370914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31291564-G-T

http://identifiers.org/hco/9/GRCh38#130370917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31291567-C-A

130370975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31291623-C-T

http://identifiers.org/hco/9/GRCh38#130371073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31291721-C-A

130371149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31291797-G-A

130371160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31291806-G-A

130371729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31291916-G-A

130371791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31291979-C-T

130371873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31292091-G-A

130372178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31292340-G-A

130372178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31292340-G-T

130372224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31292369-G-A

130372224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31292369-G-T

130372237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31292375-C-G

http://identifiers.org/hco/9/GRCh38#130372289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31292419-C-A

130372289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31292419-C-T

130372328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31292458-G-A

130372328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31292458-G-T

http://identifiers.org/hco/9/GRCh38#130372380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31292510-C-A

130372380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31292510-C-T

130372414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31292544-T-C

130372415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31292545-A-G

130372435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31292565-G-A

130372435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31292565-G-C

http://identifiers.org/hco/9/GRCh38#130372440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31292570-A-C

130372440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31292570-A-G

130372464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31292593-A-G

http://identifiers.org/hco/9/GRCh38#130372997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31293624-C-A

130372997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31293624-C-G

130373004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31293631-C-G

http://identifiers.org/hco/9/GRCh38#130373170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31293778-C-A

130373170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31293778-C-T

130373202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31293787-T-C

130373203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31293788-G-A

130373203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31293788-G-T

130373282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31293848-T-A

130373399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31293919-C-G

130373821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294216-A-G

130373852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294247-A-T

130373888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294282-A-G

130373908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294302-A-G

130373912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294306-A-G

130373972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294321-G-A

130373980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294329-G-A

130374407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294634-T-C

http://identifiers.org/hco/9/GRCh38#130374411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31294638-C-A

130374411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294638-C-T

http://identifiers.org/hco/9/GRCh38#130374426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31294650-C-A

130374439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294663-G-A

130374439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31294663-G-T

130375238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31295235-T-C

130375452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31295388-T-A

130375452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31295388-T-C

http://identifiers.org/hco/9/GRCh38#130375570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31295505-C-A

130375570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31295505-C-T

http://identifiers.org/hco/9/GRCh38#130375572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31295507-C-A

130375572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31295507-C-G

http://identifiers.org/hco/9/GRCh38#130375588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31295523-C-A

130375588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31295523-C-T

130375603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31295538-T-C

130375774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31295706-T-C

130375919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31295836-T-C

http://identifiers.org/hco/9/GRCh38#130375961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31295878-C-A

130375961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31295878-C-T

130376083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31295977-G-A

130376083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31295977-G-T

130376095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31295989-G-A

130376095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31295989-G-T

130376132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31296024-G-A

http://identifiers.org/hco/9/GRCh38#130376474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31296353-C-A

130376474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31296353-C-G

130376474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31296353-C-T

http://identifiers.org/hco/9/GRCh38#130376508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31296385-C-A

130376508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31296385-C-T

http://identifiers.org/hco/9/GRCh38#130376758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31296635-C-A

http://identifiers.org/hco/9/GRCh38#130377670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31297025-C-A

http://identifiers.org/hco/9/GRCh38#130377687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31297042-A-C

130377687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31297042-A-G

130377687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31297042-A-T

130378309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31297451-T-A

130378312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31297454-G-A

130378358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31297497-G-A

130378423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31297550-G-T

130378544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31297671-A-G

http://identifiers.org/hco/9/GRCh38#130379124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31298825-C-A

130379124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31298825-C-T

130379135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31298836-G-T

http://identifiers.org/hco/9/GRCh38#130379137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31298838-C-A

130379137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31298838-C-T

http://identifiers.org/hco/9/GRCh38#130379173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31298881-C-A

130379173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31298881-C-T

http://identifiers.org/hco/9/GRCh38#130379241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31298935-C-A

130379241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31298935-C-T

http://identifiers.org/hco/9/GRCh38#130379242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31298936-C-A

130379259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31298953-G-A

130379259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31298953-G-T

130379273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31298967-G-A

130379273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31298967-G-C

130379273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31298967-G-T

130379275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31298969-G-T

130379310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31299004-G-A

130379313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31299007-G-A

130379313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31299007-G-T

http://identifiers.org/hco/9/GRCh38#130379318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31299012-C-A

130379318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31299012-C-T

130379328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31299022-A-G

http://identifiers.org/hco/9/GRCh38#130379379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#31299073-C-A

130379379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31299073-C-T

130379420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31299114-G-A

130379424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31299118-G-A

130379424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31299118-G-T

http://identifiers.org/hco/9/GRCh38#130379522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31299177-C-A

130379565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31299201-T-C

130379565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31299201-T-G

130379592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31299228-A-G

130380228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31300146-G-A

130380241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31300159-T-C

130380326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31300240-G-A

130380358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31300314-G-A

130380457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31300407-C-G

130380961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31300528-C-T

130381048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31300596-C-G

130381157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31300687-A-G

130381710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31300903-C-T

http://identifiers.org/hco/9/GRCh38#130382088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31301168-C-A

130382088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301168-C-T

130382098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301178-G-A

130382098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301178-G-C

130382098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301178-G-T

http://identifiers.org/hco/9/GRCh38#130382121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31301198-C-A

130382121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301198-C-T

http://identifiers.org/hco/9/GRCh38#130382188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31301265-C-A

130382188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31301265-C-T

130382322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301392-G-A

http://identifiers.org/hco/9/GRCh38#130382353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31301425-C-A

130382353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301425-C-T

130382377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301449-A-T

130382384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301456-A-G

130382384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301456-A-T

http://identifiers.org/hco/9/GRCh38#130382421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31301494-C-A

130382557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301632-T-A

130382557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301632-T-C

http://identifiers.org/hco/9/GRCh38#130382659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31301714-C-A

130382659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301714-C-T

http://identifiers.org/hco/9/GRCh38#130382664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31301719-C-A

130382664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301719-C-G

130382664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301719-C-T

http://identifiers.org/hco/9/GRCh38#130382670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31301724-C-A

130382670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301724-C-T

http://identifiers.org/hco/9/GRCh38#130382672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31301726-C-A

130382672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31301726-C-T

130382876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301930-G-A

130382876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301930-G-C

130382876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301930-G-T

http://identifiers.org/hco/9/GRCh38#130382878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31301932-C-A

130382878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301932-C-T

130382896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301949-G-A

130382896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301949-G-C

130382896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301949-G-T

130382916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301969-G-A

130382916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31301969-G-T

130382959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302027-T-C

130383003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302031-A-G

130383015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302043-G-A

130383015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302043-G-T

http://identifiers.org/hco/9/GRCh38#130383016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31302044-C-A

130383016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302044-C-T

130383147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302142-G-A

130383251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302219-C-T

130383313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302270-A-T

130383373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302333-A-G

130383373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302333-A-T

130383374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302334-G-T

130383401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302360-T-C

http://identifiers.org/hco/9/GRCh38#130383415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31302382-A-C

130383415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302382-A-G

130383515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31302497-A-G

130383521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: synonymous variant
orthologous variants: 31302503-G-T

130383591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense variant
orthologous variants: 31302573-A-G

http://identifiers.org/hco/9/GRCh38#130383641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31302621-C-A

130383727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302682-A-G

130383971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31302904-G-A

130384111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31303014-T-A

130384246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 31303152-A-G

130384315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31303225-T-A

130384326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31303235-T-G

130384330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31303239-G-A

130384330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31303239-G-T

http://identifiers.org/hco/9/GRCh38#130384470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31303363-C-A

130384470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31303363-C-G

130384470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31303363-C-T

130384574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31303466-A-G

130384645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31303534-G-T

130384671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31303568-G-A

130384671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31303568-G-C

130384671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31303568-G-T

130384738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31303632-A-G

130384797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 31303691-G-T

130384890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31303795-G-A

130384890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31303795-G-T

130384904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31303825-G-A

130384904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31303825-G-C

130384904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31303825-G-T

130385312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304314-G-A

130385313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304315-G-A

130385326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304328-C-G

http://identifiers.org/hco/9/GRCh38#130385413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31304394-C-A

130385413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304394-C-T

http://identifiers.org/hco/9/GRCh38#130385414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31304395-C-A

130385414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304395-C-T

130385446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304427-G-A

130385446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304427-G-T

130385450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304431-T-C

130385473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304453-G-A

130385473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304453-G-T

http://identifiers.org/hco/9/GRCh38#130385500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31304478-C-A

130385500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304478-C-T

130385506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304484-G-A

130385506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304484-G-C

130385506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304484-G-T

130385603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31304582-G-A

130385603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31304582-G-C

130385603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31304582-G-T

130385608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31304587-T-A

130385621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31304600-G-A

http://identifiers.org/hco/9/GRCh38#130385639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31304618-C-A

130385639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31304618-C-T

130385690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31304669-G-A

130385690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31304669-G-T

http://identifiers.org/hco/9/GRCh38#130385772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31304751-C-A

130385772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304751-C-G

http://identifiers.org/hco/9/GRCh38#130385810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31304778-C-A

130385810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304778-C-G

130385810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304778-C-T

130385832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304800-G-A

130385832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304800-G-T

130385862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304822-G-A

130385862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304822-G-C

130385862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31304822-G-T

http://identifiers.org/hco/9/GRCh38#130386303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31305138-C-A

130386318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31305153-G-C

130386318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31305153-G-T

130386428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31305203-C-T

http://identifiers.org/hco/9/GRCh38#130388276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31306600-C-A

130388276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31306600-C-T

130388277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31306601-A-T

130388284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31306608-A-G

130388349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31306666-G-A

130388349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31306666-G-T

130388352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31306669-G-A

130388363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31306680-T-C

130388448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31306761-G-T

130388488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31306801-G-A

130388488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31306801-G-T

130388509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31306822-G-A

130388509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31306822-G-T

http://identifiers.org/hco/9/GRCh38#130388519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31306832-C-A

130388536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31306849-T-A

130388536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31306849-T-C

130388537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31306850-G-A

130388537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31306850-G-T

130388577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31306897-A-G

130388577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31306897-A-T

130388894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31307671-G-A

130388958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31307742-C-T

130389008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31307791-G-A

130389020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31307811-A-G

130389020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31307811-A-T

130389366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308137-T-C

130389439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308187-T-C

130389449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308197-G-A

130389556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308302-T-C

130389857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308485-G-A

http://identifiers.org/hco/9/GRCh38#130389864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31308492-C-A

130389864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308492-C-T

130389865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308493-G-A

130390115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308643-C-T

130390168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308686-G-A

130390187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308706-C-G

130390187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308706-C-T

130390271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308847-T-G

http://identifiers.org/hco/9/GRCh38#130390286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31308860-A-C

130390289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31308863-G-A

130390662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309210-A-G

130390840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309508-A-G

http://identifiers.org/hco/9/GRCh38#130390858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31309548-C-A

130390858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309548-C-G

130390858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309548-C-T

130390874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309650-G-A

130390874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309650-G-T

130390902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309756-C-T

130390903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309757-T-C

130390948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309804-G-A

http://identifiers.org/hco/9/GRCh38#130390963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31309820-C-A

130390985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31309842-G-A

130390985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31309842-G-T

130391050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31309907-G-A

130391105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31309962-G-A

130391105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31309962-G-T

130391107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31309964-G-A

130391116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31309973-G-T

130391124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309981-G-T

130391131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309988-G-A

130391131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31309988-G-T

130391146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310010-T-C

130391162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310024-G-A

130391162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310024-G-C

130391196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 31310062-T-C

130391292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31310158-G-A

130391292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31310158-G-T

http://identifiers.org/hco/9/GRCh38#130391333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31310199-C-A

130391333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31310199-C-T

130391334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31310200-G-A

130391334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31310200-G-T

130391393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310255-G-A

130391393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310255-G-C

http://identifiers.org/hco/9/GRCh38#130391468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31310328-C-A

130391504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31310364-G-A

130391624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310519-G-T

130391642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310537-A-G

130391642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310537-A-T

http://identifiers.org/hco/9/GRCh38#130391700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31310576-C-A

130391700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310576-C-T

130391701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310577-A-G

130391722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310599-A-G

130391723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310600-G-A

130391723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310600-G-T

130391777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310636-G-A

130391844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31310725-T-C

http://identifiers.org/hco/9/GRCh38#130391959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31310809-C-A

130391959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31310809-C-T

130391970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31310820-G-C

130391970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 31310820-G-T

130392041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31310891-C-T

http://identifiers.org/hco/9/GRCh38#130392059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31310909-C-A

130392059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31310909-C-T

130392104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31310954-T-C

http://identifiers.org/hco/9/GRCh38#130393158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31312557-C-A

http://identifiers.org/hco/9/GRCh38#130393248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31312651-C-A

130393248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 31312651-C-T

http://identifiers.org/hco/9/GRCh38#130393367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31312770-C-A

http://identifiers.org/hco/9/GRCh38#130393379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31312780-C-A

130393379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31312780-C-T

http://identifiers.org/hco/9/GRCh38#130393398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31312799-C-A

130393398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31312799-C-G

130393398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31312799-C-T

http://identifiers.org/hco/9/GRCh38#130393410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31312810-C-A

130393410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31312810-C-G

130393410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31312810-C-T

130393605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31312970-G-T

130393637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31313009-T-C

130393682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31313057-G-C

130393731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31313093-G-T

http://identifiers.org/hco/9/GRCh38#130393734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31313096-C-A

130393734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 31313096-C-T

130393860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31313220-G-A

http://identifiers.org/hco/9/GRCh38#130393947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#31313307-C-A

130393968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31313328-G-A

130393968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31313328-G-T

130393978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31313338-G-C

http://identifiers.org/hco/9/GRCh38#130394131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31313483-C-A

130394131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31313483-C-T

http://identifiers.org/hco/9/GRCh38#130394138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31313491-C-A

130394140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31313493-G-A

130394140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31313493-G-T

130394149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31313499-G-A

130394304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31313639-G-C

130394325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31313660-G-T

http://identifiers.org/hco/9/GRCh38#130394366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31313703-C-A

130394366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31313703-C-T

http://identifiers.org/hco/9/GRCh38#130394437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31313956-C-A

130394437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31313956-C-T

http://identifiers.org/hco/9/GRCh38#130394467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31313986-C-A

130394470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31313989-G-A

130394470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31313989-G-T

http://identifiers.org/hco/9/GRCh38#130394510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31314029-C-A

130394527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31314046-G-A

130394527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31314046-G-T

130394528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 31314047-G-T

130394587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31314106-G-A

130394619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31314130-G-T

http://identifiers.org/hco/9/GRCh38#130394918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31314195-C-A

130394918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31314195-C-G

130394918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31314195-C-T

130395035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31314217-T-A

130395112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31314294-G-A

130395112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31314294-G-T

130395440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31314594-A-G

130395896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315117-G-C

130395900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315121-G-C

130395987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31315213-G-A

130395987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31315213-G-T

130395992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31315218-C-T

http://identifiers.org/hco/9/GRCh38#130395995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31315221-C-A

130395995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31315221-C-T

130396044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31315270-G-A

130396044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31315270-G-T

130396094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315310-G-A

130396094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315310-G-C

130396094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315310-G-T

130396220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31315417-A-G

130396254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31315451-G-T

130396368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315569-T-C

130396369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315570-T-C

http://identifiers.org/hco/9/GRCh38#130396390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31315592-C-A

130396390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315592-C-G

130396390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315592-C-T

130396396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315598-G-T

130396398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315600-G-A

130396398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315600-G-C

130396398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315600-G-T

http://identifiers.org/hco/9/GRCh38#130396399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31315601-C-A

130396425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315625-G-A

130396425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315625-G-T

http://identifiers.org/hco/9/GRCh38#130396437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31315637-A-C

130396437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315637-A-G

130396437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315637-A-T

130396438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315638-G-T

130396619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315722-T-G

130396759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315857-G-A

130396856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31315953-G-T

130397446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316063-G-A

130397482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316113-A-G

130397562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 31316191-C-T

130397577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31316206-C-G

130397624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31316253-C-T

http://identifiers.org/hco/9/GRCh38#130397628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31316257-C-A

130397628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31316257-C-T

130397654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 31316283-G-A

130397666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316295-T-C

130397668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316297-G-A

130397668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316297-G-C

130397668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316297-G-T

130397753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316357-T-A

130397771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316375-G-A

130397771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316375-G-T

130398321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316593-G-A

130398321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316593-G-C

130398348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316621-G-T

http://identifiers.org/hco/9/GRCh38#130398428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31316699-C-A

http://identifiers.org/hco/9/GRCh38#130398469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31316736-C-A

http://identifiers.org/hco/9/GRCh38#130398487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31316753-C-A

130398487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31316753-C-T

http://identifiers.org/hco/9/GRCh38#130398594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31316852-C-A

130398594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 31316852-C-T

http://identifiers.org/hco/9/GRCh38#130398685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31316943-C-A

130398685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31316943-C-T

130398686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31316944-G-A

130398686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31316944-G-T

130398700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31316958-G-A

130398726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31316985-C-G

130398726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31316985-C-T

130398728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31316987-G-A

130398728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31316987-G-T

http://identifiers.org/hco/9/GRCh38#130398746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31316998-C-A

130398746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31316998-C-T

130398748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317000-G-T

130398752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317004-G-A

130398752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317004-G-C

130398752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317004-G-T

130398773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317021-G-A

130398773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317021-G-C

130398773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317021-G-T

130398782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317027-G-A

130398782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317027-G-C

130398782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317027-G-T

130398783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31317028-G-A

http://identifiers.org/hco/9/GRCh38#130399526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31318215-C-A

130399526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31318215-C-T

130399595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31318284-G-A

130399595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31318284-G-T

130399676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31318355-A-G

130399724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31318401-G-T

http://identifiers.org/hco/9/GRCh38#130399738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31318424-C-A

130399738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31318424-C-T

130399969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31318576-C-T

130400074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31318673-T-G

130400151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31318748-T-C

http://identifiers.org/hco/9/GRCh38#130400159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31318756-C-A

130400159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31318756-C-T

130400624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31318802-G-A

130400639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31318816-A-T

http://identifiers.org/hco/9/GRCh38#130400713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31318904-C-A

130400713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31318904-C-T

130400799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31318983-C-G

130400799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31318983-C-T

http://identifiers.org/hco/9/GRCh38#130400963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31319147-C-A

130400963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31319147-C-T

130401035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31319211-G-C

130401035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31319211-G-T

130401126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31319289-C-G

130401220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31319374-G-A

130402137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31319774-T-C

130402205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31319891-G-T

130402353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320014-G-A

130402400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320046-T-C

130402436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320065-G-A

130402458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320068-G-A

130402765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320311-C-G

130402765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320311-C-T

130402823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31320385-C-T

130402902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320464-G-A

130402922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320484-G-C

130402948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320506-G-A

130402948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320506-G-T

130402974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320532-G-A

130402974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320532-G-T

130403109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320671-C-T

130403135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320694-G-A

130403190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31320723-G-A

130403190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31320723-G-T

130403312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31320845-G-A

130403312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31320845-G-T

130403357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320883-A-G

http://identifiers.org/hco/9/GRCh38#130403402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31320908-C-A

130403402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320908-C-T

http://identifiers.org/hco/9/GRCh38#130403413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31320919-A-C

130403424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320933-A-G

130403430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320938-T-C

130403596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31320981-G-A

130403709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31321057-C-G

130403766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31321119-C-T

130403787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31321140-T-A

130403908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31321259-G-A

130403908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31321259-G-T

http://identifiers.org/hco/9/GRCh38#130403935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31321288-C-A

130404283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31321600-G-T

130404364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31321666-G-A

130404365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31321667-G-A

130404397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31321702-T-G

130404423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31321714-C-T

130404817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322107-G-T

130405123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322415-T-A

130405128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322420-T-A

130405128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322420-T-C

130405128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322420-T-G

130405184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322467-G-A

130405184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322467-G-T

130405193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322473-C-G

130405193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322473-C-T

130405323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322644-C-G

130405323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322644-C-T

130405419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322740-G-T

130405495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31322808-A-T

130405798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31323141-G-A

http://identifiers.org/hco/9/GRCh38#130405890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31323221-C-A

130405890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31323221-C-T

130405891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31323222-A-G

130406010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31323342-G-A

http://identifiers.org/hco/9/GRCh38#130406113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31323445-C-A

130406152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31323484-C-T

130406224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323553-A-G

130406261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323589-G-C

130406261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323589-G-T

130406266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323594-A-T

http://identifiers.org/hco/9/GRCh38#130406277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31323605-C-A

130406279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323607-G-A

130406279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323607-G-T

130406320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323641-G-A

130406320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323641-G-C

130406352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323671-G-A

130406352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323671-G-T

130406374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323693-G-A

130406374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323693-G-T

130406499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323782-G-A

130406499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323782-G-T

130406521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323806-G-A

130406602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323877-G-T

http://identifiers.org/hco/9/GRCh38#130406620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31323894-C-A

http://identifiers.org/hco/9/GRCh38#130406697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31323961-C-A

130406698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323962-T-C

130406704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323968-G-A

130406704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323968-G-T

130406723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323987-G-A

130406725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31323989-T-C

130406815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31324048-G-A

130406817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31324050-G-T

http://identifiers.org/hco/9/GRCh38#130406851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324074-C-A

130406851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31324074-C-T

130406889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31324114-T-C

http://identifiers.org/hco/9/GRCh38#130407048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324186-C-A

130407048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31324186-C-T

http://identifiers.org/hco/9/GRCh38#130407105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324212-C-A

130407105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31324212-C-T

130407119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31324226-A-G

130407119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31324226-A-T

130407135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31324242-A-G

http://identifiers.org/hco/9/GRCh38#130407149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324254-C-A

130407149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31324254-C-T

http://identifiers.org/hco/9/GRCh38#130407327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324439-A-C

130407338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324450-C-G

http://identifiers.org/hco/9/GRCh38#130407386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324481-C-A

130407386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324481-C-T

130407424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324529-T-C

http://identifiers.org/hco/9/GRCh38#130407428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324533-A-C

130407428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324533-A-G

http://identifiers.org/hco/9/GRCh38#130407431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324536-A-C

130407431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324536-A-G

130407436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324541-G-A

130407436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324541-G-C

130407436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324541-G-T

130407437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324542-T-A

130407437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324542-T-C

http://identifiers.org/hco/9/GRCh38#130407459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324564-C-A

130407459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324564-C-G

130407459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324564-C-T

130407460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324565-G-A

130407460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324565-G-T

130407479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324589-G-A

130407479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324589-G-T

http://identifiers.org/hco/9/GRCh38#130407505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324616-C-A

130407505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324616-C-T

130407645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31324770-G-A

130407656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31324781-G-A

130407656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31324781-G-C

http://identifiers.org/hco/9/GRCh38#130407698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324823-C-A

130407698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31324823-C-T

http://identifiers.org/hco/9/GRCh38#130407712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324843-C-A

130407712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 31324843-C-T

http://identifiers.org/hco/9/GRCh38#130407738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324862-A-C

http://identifiers.org/hco/9/GRCh38#130407838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324955-C-A

130407838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324955-C-T

http://identifiers.org/hco/9/GRCh38#130407849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31324966-C-A

130407849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31324966-C-T

130408139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31325182-A-G

130408442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31325453-A-T

130410323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328018-T-A

130410352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328047-C-T

130410375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328069-G-A

130410474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328159-C-T

130410503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328200-A-G

130410540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328229-A-T

130410543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328235-A-G

http://identifiers.org/hco/9/GRCh38#130410547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31328239-C-A

130410547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328239-C-T

http://identifiers.org/hco/9/GRCh38#130410555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31328247-C-A

130410555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328247-C-T

130410556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328248-T-C

http://identifiers.org/hco/9/GRCh38#130410581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31328270-C-A

130410581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31328270-C-G

130410581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31328270-C-T

130410587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31328276-G-A

130410587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31328276-G-C

130410604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31328293-G-A

130410604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 31328293-G-T

130410609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31328298-T-G

130410631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31328320-G-A

130410631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31328320-G-C

130410709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31328407-G-T

130418636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31334969-G-A

130418636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31334969-G-T

130418637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31334970-G-T

http://identifiers.org/hco/9/GRCh38#130418647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31334980-C-A

130418647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31334980-C-G

130418647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31334980-C-T

130418655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31334988-G-T

http://identifiers.org/hco/9/GRCh38#130418708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31335029-C-A

130418708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31335029-C-T

130418710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31335031-T-C

http://identifiers.org/hco/9/GRCh38#130418717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31335038-C-A

130418799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31335113-A-G

130418831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31335145-G-A

http://identifiers.org/hco/9/GRCh38#130418844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31335158-A-C

130418844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31335158-A-G

130418866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31335180-C-G

130418866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31335180-C-T

130418913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31335227-G-A

130418913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31335227-G-T

http://identifiers.org/hco/9/GRCh38#130418938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31335252-C-A

http://identifiers.org/hco/9/GRCh38#130418989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31335303-C-A

130418989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31335303-C-G

130418989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31335303-C-T

http://identifiers.org/hco/9/GRCh38#130419034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31335348-C-A

130419034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31335348-C-G

130419034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 31335348-C-T

130419035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31335349-G-A

130419035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 31335349-G-T

http://identifiers.org/hco/9/GRCh38#130419050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31335364-C-A

130419050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335364-C-T

130419069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335381-G-A

130419125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335422-T-A

130419125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335422-T-C

130419133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335430-G-A

130419133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335430-G-T

130419170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335466-A-G

130419312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335619-C-G

130419312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335619-C-T

130419360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335667-G-A

130419360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335667-G-T

130419441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335744-G-A

130419568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31335872-G-T

http://identifiers.org/hco/9/GRCh38#130419581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31335885-C-A

130419643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31335947-T-G

130419737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31336031-C-T

130419796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31336088-A-G

130420071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31336324-T-C

130420805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron variant
orthologous variants: 31337084-A-G

130421468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31339145-T-G

130421485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31339170-G-T

130422174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31339787-G-C

http://identifiers.org/hco/9/GRCh38#130422472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31340710-C-A

130422472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340710-C-T

http://identifiers.org/hco/9/GRCh38#130422481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31340719-A-C

130422481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340719-A-G

130422491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340729-T-C

130422493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340731-A-G

http://identifiers.org/hco/9/GRCh38#130422494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31340732-C-A

130422494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340732-C-T

http://identifiers.org/hco/9/GRCh38#130422497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31340735-A-C

130422497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340735-A-G

130422502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340737-G-A

http://identifiers.org/hco/9/GRCh38#130422511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31340746-C-A

130422511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340746-C-T

130422513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340752-T-C

130422513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340752-T-G

130422526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340765-G-A

130422526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340765-G-T

130422538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340777-G-T

130422559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31340802-T-C

130422577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31340820-G-A

130422577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31340820-G-T

http://identifiers.org/hco/9/GRCh38#130422593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31340836-C-A

130422593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 31340836-C-T

130422595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 31340838-G-A

130422595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340838-G-T

130422651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340894-A-G

http://identifiers.org/hco/9/GRCh38#130422689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31340932-C-A

130422689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31340932-C-T

130422710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31340953-T-C

130422738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340982-G-A

130422738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31340982-G-T

130422805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31341012-T-C

130422901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31341075-C-G

130422982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31341148-T-C

130422987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31341154-C-T

130423036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31341199-A-G

130424732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31342777-T-C

130424733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31342778-G-A

130424733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31342778-G-T

130424741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31342787-G-A

http://identifiers.org/hco/9/GRCh38#130424754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31342800-C-A

130424754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31342800-C-T

http://identifiers.org/hco/9/GRCh38#130424804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31342850-C-A

130424840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31342886-T-C

130424840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31342886-T-G

130424847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31342893-G-A

130424847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31342893-G-C

130424847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31342893-G-T

130424937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31342983-G-T

130424987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31343033-G-A

130424987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31343033-G-C

130424987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31343033-G-T

http://identifiers.org/hco/9/GRCh38#130424988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31343034-C-A

130425016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31343062-G-A

http://identifiers.org/hco/9/GRCh38#130425021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31343067-C-A

130425021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 31343067-C-T

130425067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31343113-C-G

130425265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343244-T-A

130425265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343244-T-C

130425265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343244-T-G

130425267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343246-G-A

130425267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343246-G-T

130425362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343313-T-C

130425460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343345-C-T

http://identifiers.org/hco/9/GRCh38#130425539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31343369-C-A

130425584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343372-T-C

130425643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343385-T-A

130425643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343385-T-C

130425643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343385-T-G

130425749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31343457-C-T

130425932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31343640-C-T

http://identifiers.org/hco/9/GRCh38#130425960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31343663-C-A

130425960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343663-C-T

http://identifiers.org/hco/9/GRCh38#130425964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31343667-C-A

130425964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343667-C-G

130425973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343674-G-A

130425973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343674-G-T

http://identifiers.org/hco/9/GRCh38#130426004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31343699-C-A

130426004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31343699-C-G

130426004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31343699-C-T

http://identifiers.org/hco/9/GRCh38#130426005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31343700-C-A

130426005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31343700-C-T

http://identifiers.org/hco/9/GRCh38#130426025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31343703-A-C

130426025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343703-A-T

130426028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343706-G-A

130426028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343706-G-T

130426068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31343726-G-A

130426068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31343726-G-T

http://identifiers.org/hco/9/GRCh38#130426111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31343767-C-A

130426111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343767-C-G

130426111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343767-C-T

130426270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343908-C-T

http://identifiers.org/hco/9/GRCh38#130426271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31343909-A-C

130426376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344000-A-G

130426407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344012-G-A

130426546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344130-G-A

130426568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344159-G-A

130426568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344159-G-C

130426717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344292-A-G

130426811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344327-A-T

130427107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31344429-A-G

130427167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31344490-G-A

130427167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31344490-G-T

http://identifiers.org/hco/9/GRCh38#130427204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#31344517-C-A

130427204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31344517-C-G

130427204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31344517-C-T

130427254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344566-G-A

130427355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 31344682-C-T

130427356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 31344683-C-G

130427634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344953-G-A

130427634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344953-G-T

130427642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344961-G-A

130427666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31344973-G-A

http://identifiers.org/hco/9/GRCh38#130427734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31345040-C-A

130427734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345040-C-T

130427740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345046-T-A

130427740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345046-T-C

130427859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345086-G-A

130427880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345097-G-T

http://identifiers.org/hco/9/GRCh38#130427958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31345153-C-A

130427958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345153-C-T

130427986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345182-G-T

http://identifiers.org/hco/9/GRCh38#130428235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31345406-C-A

130428235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345406-C-T

130428253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345424-T-C

130428351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31345497-C-T

130428374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31345520-G-A

130428374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31345520-G-T

130428378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31345524-G-A

130428381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31345527-G-T

http://identifiers.org/hco/9/GRCh38#130428428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31345574-C-A

130428452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31345598-G-A

130428452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31345598-G-T

130428467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31345616-G-T

130428496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31345645-G-A

130428496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31345645-G-T

http://identifiers.org/hco/9/GRCh38#130428500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31345649-C-A

130428500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345649-C-T

http://identifiers.org/hco/9/GRCh38#130428505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31345654-C-A

130428505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345654-C-T

130428516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345665-T-A

130428516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345665-T-C

130428517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345666-C-G

130428517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345666-C-T

http://identifiers.org/hco/9/GRCh38#130428518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31345667-C-A

130428518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345667-C-T

130428579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345699-G-A

130428579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345699-G-T

http://identifiers.org/hco/9/GRCh38#130428605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31345718-C-A

130428605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345718-C-G

130428872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345895-C-T

130428937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345960-G-A

130428937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345960-G-C

130429139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31346472-T-A

130429139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31346472-T-C

130429140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31346473-G-A

130429140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31346473-G-C

130429140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31346473-G-T

http://identifiers.org/hco/9/GRCh38#130429196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31346529-C-A

130429271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31346592-A-G

http://identifiers.org/hco/9/GRCh38#130429347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31346627-C-A

130429347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31346627-C-T

130429387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31346666-A-G

http://identifiers.org/hco/9/GRCh38#130429459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31346966-C-A

130429459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31346966-C-T

130429480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31346987-G-A

130429480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31346987-G-T

http://identifiers.org/hco/9/GRCh38#130429492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31346999-C-A

130429492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31346999-C-T

130429509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347014-G-A

130429509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347014-G-C

130429846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347285-T-C

130429873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347313-A-G

130429873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347313-A-T

130429901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347332-G-A

130429901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347332-G-T

http://identifiers.org/hco/9/GRCh38#130429902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31347333-C-A

130429902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347333-C-T

130429981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347406-G-A

130429981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347406-G-T

130430049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347490-A-G

130430230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347697-G-A

130430230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347697-G-T

130430255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347717-T-G

http://identifiers.org/hco/9/GRCh38#130430281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31347742-C-A

130430452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347913-G-A

130430452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347913-G-T

130430489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31347950-C-G

130430489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31347950-C-T

130430671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348118-G-A

130430671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348118-G-T

130430712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348153-A-G

130430735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348168-G-T

130430745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348179-G-A

130430745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348179-G-T

130430808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348239-G-T

130430815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348248-A-G

http://identifiers.org/hco/9/GRCh38#130430910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31348349-C-A

130430910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348349-C-G

130430910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348349-C-T

130430951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348369-A-G

130430951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348369-A-T

130430953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348371-G-A

130430953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348371-G-T

130431009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348425-G-A

130431009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348425-G-T

130431010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348426-A-G

130431010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348426-A-T

130431096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348492-T-C

130431096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348492-T-G

130431142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348513-T-C

130431144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348515-T-C

130431227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348571-G-A

130431227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348571-G-T

130431236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348580-G-A

http://identifiers.org/hco/9/GRCh38#130431244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31348588-A-C

130431244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348588-A-G

130431249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348593-G-A

130431249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348593-G-T

130431426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31348755-A-T

130431440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31348769-G-A

130431485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31348814-G-T

http://identifiers.org/hco/9/GRCh38#130431621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31348983-C-A

130431621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31348983-C-T

130432403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31349077-C-T

130432580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31349248-C-T

130432644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349304-T-C

130432644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349304-T-G

130432659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349367-T-C

130432659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349367-T-G

130432664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349372-G-A

130432664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349372-G-T

130432685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31349387-G-C

130432685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31349387-G-T

130432695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349397-G-A

130432695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349397-G-C

130432695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349397-G-T

130432707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349421-G-T

130432712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349426-G-A

130432712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349426-G-T

130432726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349448-G-A

http://identifiers.org/hco/9/GRCh38#130432756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31349487-C-A

130432756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349487-C-T

130432900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349641-T-A

130432900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349641-T-C

130432900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349641-T-G

130432940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349666-A-G

130432962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349687-G-A

130432962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349687-G-T

http://identifiers.org/hco/9/GRCh38#130432996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31349718-A-C

130432996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349718-A-G

http://identifiers.org/hco/9/GRCh38#130433032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31349748-C-A

http://identifiers.org/hco/9/GRCh38#130433114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31349884-C-A

130433114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349884-C-G

130433114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349884-C-T

130433143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349924-G-A

130433143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349924-G-T

130433167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349948-G-C

130433167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31349948-G-T

130433429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 31350143-G-A

130433429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 31350143-G-T

http://identifiers.org/hco/9/GRCh38#130433520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31350234-C-A

130433520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31350234-C-G

130433520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31350234-C-T

130433652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31350366-G-A

130433652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31350366-G-T

http://identifiers.org/hco/9/GRCh38#130433669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31350383-C-A

130433669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31350383-C-T

130433766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350469-C-T

http://identifiers.org/hco/9/GRCh38#130433778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31350481-C-A

130433778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350481-C-T

http://identifiers.org/hco/9/GRCh38#130433943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31350615-C-A

130433943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350615-C-G

130433943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350615-C-T

130433965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350634-T-A

130433965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350634-T-C

130433965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350634-T-G

130433988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350647-C-G

130433988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350647-C-T

130434047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350687-A-G

130434093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350720-T-G

http://identifiers.org/hco/9/GRCh38#130434098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#31350725-A-C

130434109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350736-T-A

130434109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350736-T-C

130434109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350736-T-G

130434110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350737-T-C

130434112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21293
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31350739-T-C