215360790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71624592-T-C

215360835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71624645-T-C

http://identifiers.org/hco/2/GRCh38#215360839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71624649-A-C

215360839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71624649-A-G

215360839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71624649-A-T

http://identifiers.org/hco/2/GRCh38#215360855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71624671-C-A

215360855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71624671-C-T

http://identifiers.org/hco/2/GRCh38#215360946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71624761-C-A

215360960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71624775-C-T

215360985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71624800-T-A

215360992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71624807-T-C

http://identifiers.org/hco/2/GRCh38#215361232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71625045-C-A

215361244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71625056-G-A

215361244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71625056-G-T

http://identifiers.org/hco/2/GRCh38#215361342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71625160-C-A

215361342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71625160-C-T

215361378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71625196-A-G

215361398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71625217-G-A

215361415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71625234-A-G

http://identifiers.org/hco/2/GRCh38#215361593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71625409-A-C

http://identifiers.org/hco/2/GRCh38#215361653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71625463-A-C

215361693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71625504-G-T

215361723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71625543-T-A

215361723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71625543-T-C

215361723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71625543-T-G

215361745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71625556-C-T

http://identifiers.org/hco/2/GRCh38#215361746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71625557-C-A

215361746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71625557-C-G

215361851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71625681-T-C

215361896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71625901-T-A

215361896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71625901-T-C

215361930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71625959-T-C

215361986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626006-G-A

215361986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626006-G-T

215362098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626119-G-T

215362110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626131-G-A

215362110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626131-G-C

215362110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626131-G-T

215362112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626133-T-C

215362150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626163-G-A

215362150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626163-G-T

215362186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626186-A-G

215362186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626186-A-T

215362189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626189-T-C

215362189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626189-T-G

215362224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626220-T-G

215362230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626226-G-A

215362230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626226-G-C

215362230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626226-G-T

215362246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626244-A-G

http://identifiers.org/hco/2/GRCh38#215362308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71626288-C-A

http://identifiers.org/hco/2/GRCh38#215362370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71626334-C-A

http://identifiers.org/hco/2/GRCh38#215362373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71626337-C-A

215362381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626348-A-G

215362467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626438-T-C

215362540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626489-A-G

215362547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626496-A-T

215362558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626507-A-G

http://identifiers.org/hco/2/GRCh38#215362624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71626537-C-A

http://identifiers.org/hco/2/GRCh38#215362662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71626574-C-A

215362685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626597-T-A

http://identifiers.org/hco/2/GRCh38#215362811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71626705-A-C

215362811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626705-A-G

http://identifiers.org/hco/2/GRCh38#215362819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71626708-C-A

215362819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626708-C-T

http://identifiers.org/hco/2/GRCh38#215362826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71626715-C-A

215362826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626715-C-T

215362874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626774-G-T

http://identifiers.org/hco/2/GRCh38#215362881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71626781-C-A

215362881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71626781-C-T

215363242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71627221-G-T

215363286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71627265-T-C

215363390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71627349-G-C

215363390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71627349-G-T

http://identifiers.org/hco/2/GRCh38#215363579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71627709-C-A

215363644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71627797-A-G

215363728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71628056-G-A

215364308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71628672-T-A

215364308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71628672-T-G

215364444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71628795-G-T

215364800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71629192-T-C

215364873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71629251-T-C

http://identifiers.org/hco/2/GRCh38#215364927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71629305-C-A

215364927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71629305-C-T

215364948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71629326-G-A

215364948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71629326-G-T

215364954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71629332-T-A

215364954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71629332-T-C

http://identifiers.org/hco/2/GRCh38#215364963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71629341-A-C

215364963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71629341-A-G

215364963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71629341-A-T

http://identifiers.org/hco/2/GRCh38#215364966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71629344-A-C

215364966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71629344-A-G

215364972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 71629350-A-T

http://identifiers.org/hco/2/GRCh38#215365007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71629389-A-C

215365007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71629389-A-T

http://identifiers.org/hco/2/GRCh38#215365014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71629396-C-A

215365014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71629396-C-T

215365086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71629459-C-T

215365291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71629737-T-C

215365533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71629954-G-A

215365614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71630035-A-G

http://identifiers.org/hco/2/GRCh38#215365727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71630129-C-A

http://identifiers.org/hco/2/GRCh38#215365766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71630169-C-A

215365766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71630169-C-G

215366267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71630289-A-T

215366395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71630397-T-C

215366416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71630486-C-T

215366446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71630516-A-T

215366483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71630568-A-G

215366713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71630860-G-A

215366737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71630879-G-C

215367108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71631185-A-T

215367314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71631390-G-T

215367413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71631769-A-G

215367590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71631949-G-T

215367597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71631961-T-G

215367745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71632109-T-A

215367770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71632134-T-C

215367770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71632134-T-G

215367792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71632156-T-C

215367846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71632212-A-G

215367939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71632306-T-C

215367948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71632315-C-T

http://identifiers.org/hco/2/GRCh38#215368052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71632419-A-C

215368063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71632436-T-C

215368063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71632436-T-G

http://identifiers.org/hco/2/GRCh38#215368161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71632517-C-A

215368161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71632517-C-G

http://identifiers.org/hco/2/GRCh38#215368255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71632585-C-A

215368297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71632599-T-C

215368505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71632781-A-G

http://identifiers.org/hco/2/GRCh38#215368523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71632799-C-A

http://identifiers.org/hco/2/GRCh38#215368599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71632886-A-C

215368620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71632907-C-T

215369066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633342-A-G

215369234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633543-T-A

215369235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633544-G-A

215369235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633544-G-T

215369371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71633665-A-G

215369746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634324-T-C

215369917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634527-G-A

215369977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634579-A-G

215370173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634712-T-C

215370212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634744-A-G

215370214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634746-A-G

215370265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71634792-C-T

215370480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71634999-G-T

215370484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71635004-G-C

215370484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71635004-G-T

215370534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635057-G-A

215370534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635057-G-C

215370534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635057-G-T

215370580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635080-T-A

215370580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635080-T-G

http://identifiers.org/hco/2/GRCh38#215370587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71635087-C-A

215370593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635093-C-T

215370623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635124-G-C

215370623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635124-G-T

http://identifiers.org/hco/2/GRCh38#215370877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71635538-C-A

215370980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635642-A-T

215371369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635721-T-C

215371556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71635887-A-G

215371614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636008-A-G

215371732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636182-T-C

215371745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636195-T-A

215371750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636200-T-A

http://identifiers.org/hco/2/GRCh38#215371754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71636204-C-A

215371769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636219-T-A

215371769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636219-T-C

http://identifiers.org/hco/2/GRCh38#215371773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71636223-A-C

215371782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636232-G-T

http://identifiers.org/hco/2/GRCh38#215371784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71636234-A-C

215371784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636234-A-G

215371784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636234-A-T

http://identifiers.org/hco/2/GRCh38#215371787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71636237-A-C

215371787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71636237-A-T

215372070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71636601-C-T

215372140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71636671-C-T

215372287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71636818-A-G

215372470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71637000-T-A

215372486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637016-A-G

http://identifiers.org/hco/2/GRCh38#215372580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71637115-A-C

215372580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637115-A-G

215373040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637296-G-C

215373182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637422-A-G

215373195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637435-T-A

215373195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637435-T-C

http://identifiers.org/hco/2/GRCh38#215373217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71637462-C-A

215373217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637462-C-G

215373217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637462-C-T

215373440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637651-T-C

215373440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637651-T-G

215373447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637658-G-C

215373447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71637658-G-T

http://identifiers.org/hco/2/GRCh38#215373489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71637688-C-A

215375008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638190-A-G

215375039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638221-C-G

215375178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638341-G-A

215375178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638341-G-C

215375178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638341-G-T

http://identifiers.org/hco/2/GRCh38#215375184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71638347-A-C

215375185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638348-G-A

215375380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71638540-T-C

215375467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638616-C-T

215375491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638645-T-A

215375491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638645-T-C

215375494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638648-G-A

215375570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638701-G-T

http://identifiers.org/hco/2/GRCh38#215375777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71638908-A-C

http://identifiers.org/hco/2/GRCh38#215375829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71638949-C-A

215375859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71638968-A-T

215375898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639008-A-G

215375898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639008-A-T

215376117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639061-A-G

215376289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639238-G-A

215376380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639356-G-A

215376380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639356-G-T

215376387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639363-T-C

215376472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639428-G-A

215376705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639656-C-T

215376732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639683-G-A

215376732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639683-G-T

http://identifiers.org/hco/2/GRCh38#215376789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71639738-A-C

http://identifiers.org/hco/2/GRCh38#215376791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71639740-C-A

215376791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639740-C-G

215376841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639776-G-A

215376862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71639797-A-T

215378145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640321-T-C

215378145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640321-T-G

215378147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640323-G-A

215378147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640323-G-T

215378185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71640370-G-T

215378201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71640386-G-A

215378201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71640386-G-T

215378217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71640402-A-G

215378254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71640439-G-C

215378254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71640439-G-T

215378279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640462-A-T

http://identifiers.org/hco/2/GRCh38#215378315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71640496-A-C

215378315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640496-A-T

215378327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640509-A-T

http://identifiers.org/hco/2/GRCh38#215378387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71640569-A-C

http://identifiers.org/hco/2/GRCh38#215378562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71640744-C-A

215378597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71640784-A-G

http://identifiers.org/hco/2/GRCh38#215378914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71641255-A-C

215379004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641355-A-G

215379053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641404-T-C

215379119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641458-T-G

215379124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71641463-T-C

215379187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71641526-T-C

215379359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641699-T-C

http://identifiers.org/hco/2/GRCh38#215379387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71641726-C-A

215379387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641726-C-T

215379414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641753-G-T

215379472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641800-G-A

215379472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641800-G-T

215379473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641801-G-A

215379473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641801-G-T

215379483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641811-T-A

215379483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641811-T-C

215379483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641811-T-G

215379618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641931-C-G

215379618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71641931-C-T

215380146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642138-C-T

http://identifiers.org/hco/2/GRCh38#215380256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71642227-A-C

215380336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642302-G-A

http://identifiers.org/hco/2/GRCh38#215380348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71642314-A-C

215380348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642314-A-G

215380392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642358-G-T

http://identifiers.org/hco/2/GRCh38#215380410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71642372-C-A

215380410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642372-C-T

215380411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642373-G-A

215380411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642373-G-C

215380411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642373-G-T

215380519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642486-A-G

215380590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642581-G-A

215380590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642581-G-T

http://identifiers.org/hco/2/GRCh38#215380609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71642600-A-C

215380609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642600-A-G

215380641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642631-A-G

215380677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642667-T-A

215380677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642667-T-C

http://identifiers.org/hco/2/GRCh38#215380689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71642679-C-A

215380690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642680-T-A

215380690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642680-T-C

http://identifiers.org/hco/2/GRCh38#215380693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71642687-C-A

215380693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71642687-C-G

215381171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71643182-A-G

215381219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71643235-C-G

http://identifiers.org/hco/2/GRCh38#215381268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71643295-A-C

215381268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71643295-A-G

215381332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71643362-G-T

http://identifiers.org/hco/2/GRCh38#215381534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71643568-C-A

215381546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71643580-T-C

http://identifiers.org/hco/2/GRCh38#215381562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71643601-C-A

215381562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71643601-C-T

http://identifiers.org/hco/2/GRCh38#215381564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71643603-C-A

http://identifiers.org/hco/2/GRCh38#215381830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71643759-C-A

215381899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71643820-T-G

http://identifiers.org/hco/2/GRCh38#215382040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71643960-C-A

215382040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71643960-C-G

215382040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71643960-C-T

http://identifiers.org/hco/2/GRCh38#215382047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71643968-C-A

215382047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 71643968-C-T

215382077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71643989-G-A

215382077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71643989-G-T

215382249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71644166-G-A

215382249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71644166-G-C

215382279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71644196-A-G

215382288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71644205-T-G

215382355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644268-A-G

http://identifiers.org/hco/2/GRCh38#215382360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71644273-C-A

215382360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644273-C-T

http://identifiers.org/hco/2/GRCh38#215382379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71644287-C-A

215382379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644287-C-G

215382379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644287-C-T

215382389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644297-G-A

215382389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644297-G-T

215382457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644378-G-C

215382457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644378-G-T

215382468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644389-T-C

215382548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644424-C-T

215382740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644601-C-G

215382740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71644601-C-T

215383365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71645081-A-G

215383532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645241-C-G

215383532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645241-C-T

215383583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645292-C-G

215383652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645372-T-G

http://identifiers.org/hco/2/GRCh38#215383655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71645375-A-C

215383770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645493-G-T

215383783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645505-G-A

215383783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645505-G-T

215383804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645530-C-T

215383822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645548-C-T

http://identifiers.org/hco/2/GRCh38#215383898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71645626-C-A

215383898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645626-C-T

215383907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645635-G-A

215383907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645635-G-C

215383907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645635-G-T

215383934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645781-C-G

http://identifiers.org/hco/2/GRCh38#215383964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71645811-C-A

215383996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71645840-T-G

215384042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71645884-T-C

http://identifiers.org/hco/2/GRCh38#215384269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71646097-C-A

215384269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646097-C-T

215384270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646098-A-G

http://identifiers.org/hco/2/GRCh38#215384301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71646129-C-A

215384341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646179-G-T

http://identifiers.org/hco/2/GRCh38#215384353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71646191-C-A

215384400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646238-T-A

215384544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646678-A-T

http://identifiers.org/hco/2/GRCh38#215384594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71646720-C-A

215384610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646734-G-T

215384655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646775-A-G

215384668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646788-A-G

http://identifiers.org/hco/2/GRCh38#215384714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71646829-C-A

215384714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646829-C-T

215384740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646950-G-A

215384740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646950-G-T

215384741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646951-G-A

215384741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646951-G-T

215384747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646957-G-A

215384747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71646957-G-T

215384870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71647073-G-A

215384870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 71647073-G-T

215384932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71647135-T-C

http://identifiers.org/hco/2/GRCh38#215385006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71647215-C-A

215385006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71647215-C-T

215385122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71647329-T-C

215385124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71647331-A-T

215386613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648487-A-G

http://identifiers.org/hco/2/GRCh38#215386621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71648495-C-A

215386621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648495-C-T

215386743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71648626-C-T

215386846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71648729-G-A

215387028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648903-A-G

215387030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648905-G-T

215387032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648907-G-A

215387032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71648907-G-T

http://identifiers.org/hco/2/GRCh38#215388091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71649993-C-A

215388091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649993-C-T

215388096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649998-G-A

215388096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71649998-G-T

http://identifiers.org/hco/2/GRCh38#215388105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71650006-C-A

215388167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650069-G-C

215388167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650069-G-T

215388203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650079-A-G

http://identifiers.org/hco/2/GRCh38#215388246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71650122-A-C

215388246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71650122-A-G

215388246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71650122-A-T

215388279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71650155-A-G

215388305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71650181-T-A

215388305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71650181-T-C

http://identifiers.org/hco/2/GRCh38#215388357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71650232-A-C

215388375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650251-T-C

http://identifiers.org/hco/2/GRCh38#215388395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71650271-A-C

215388395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650271-A-G

215388398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650274-G-A

215388398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650274-G-T

215388435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650311-T-C

http://identifiers.org/hco/2/GRCh38#215388437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71650313-C-A

215388498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650343-A-G

215388666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650490-T-C

http://identifiers.org/hco/2/GRCh38#215388728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71650535-C-A

215390580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650725-T-C

215390703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650836-C-T

215390780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71650885-G-A

215391005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651061-T-C

215391048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651100-T-C

http://identifiers.org/hco/2/GRCh38#215391135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71651181-C-A

215391345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651349-T-A

215391414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651411-C-T

215391520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71651503-T-A

215391520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71651503-T-C

215391520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71651503-T-G

215391573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651557-G-T

215391599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71651593-A-G

215391681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 71651676-A-G

215391937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71651933-A-G

215392063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652063-A-G

215392063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652063-A-T

http://identifiers.org/hco/2/GRCh38#215392079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71652080-A-C

215392099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652123-A-G

215392132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652154-G-A

215392132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652154-G-C

215392132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652154-G-T

http://identifiers.org/hco/2/GRCh38#215392194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71652214-C-A

215392194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652214-C-G

215392194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652214-C-T

215392226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652246-C-G

http://identifiers.org/hco/2/GRCh38#215392250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71652281-C-A

215392250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652281-C-G

215392250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652281-C-T

http://identifiers.org/hco/2/GRCh38#215392428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71652456-A-C

215392455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652482-A-G

http://identifiers.org/hco/2/GRCh38#215392459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71652486-C-A

215392459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652486-C-T

http://identifiers.org/hco/2/GRCh38#215392522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71652541-A-C

215392522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652541-A-T

http://identifiers.org/hco/2/GRCh38#215392544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71652561-A-C

215392544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652561-A-G

215392610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652628-T-A

215392610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652628-T-G

215392737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652744-T-C

215392737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652744-T-G

215392742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652749-A-G

http://identifiers.org/hco/2/GRCh38#215392750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71652757-C-A

215392750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652757-C-T

215392780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652783-T-C

215392806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652803-C-G

215392824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652821-T-C

215392858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652851-T-C

215392858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652851-T-G

215392870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71652863-G-A

http://identifiers.org/hco/2/GRCh38#215393215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71653206-C-A

215393284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71653271-A-T

http://identifiers.org/hco/2/GRCh38#215393342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71653328-C-A

215393344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71653330-G-A

215393344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71653330-G-T

215393400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71653386-A-G

215393450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71653425-T-G

215393837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71653816-C-T

215394251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71654242-T-C

215394448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71654439-A-G

215394448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71654439-A-T

215394457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71654447-G-C

http://identifiers.org/hco/2/GRCh38#215394471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71654461-A-C

215394538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71654529-G-A

215394538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71654529-G-C

215394736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71654727-A-G

http://identifiers.org/hco/2/GRCh38#215394749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71654740-C-A

215394749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71654740-C-T

215394783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71654774-A-G

http://identifiers.org/hco/2/GRCh38#215395178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71655217-C-A

215395622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71655365-A-G

215395708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71655445-C-T

215395767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71655506-A-T

215396125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71655858-T-C

215396179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71656551-G-T

215396927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71657525-G-T

http://identifiers.org/hco/2/GRCh38#215397008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71657600-A-C

215397008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71657600-A-G

215397014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71657606-T-G

215397026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71657618-T-G

215397101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71657676-G-A

215397101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71657676-G-T

215397131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71657707-A-G

215397269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71657873-T-G

http://identifiers.org/hco/2/GRCh38#215397341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71657968-A-C

215397416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71658037-G-C

215397609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71658223-T-C

215397612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71658226-A-G

215397792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71658655-T-G

215397886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71658749-T-C

215397889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71658751-T-C

215397909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71658763-T-C

215397910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71658764-G-T

215397956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71658805-G-A

215397956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71658805-G-T

215397963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71658812-G-T

http://identifiers.org/hco/2/GRCh38#215397991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71658842-C-A

215398072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71658911-G-A

215398114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71658947-G-T

215398518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659192-A-G

215398596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659283-G-T

215398909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659608-T-A

215398950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659649-T-C

215399119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659777-T-C

http://identifiers.org/hco/2/GRCh38#215399196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71659827-A-C

215399200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659831-G-T

215399230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659861-C-T

215399243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659870-C-T

215399246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659873-C-G

215399246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659873-C-T

http://identifiers.org/hco/2/GRCh38#215399250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71659877-A-C

215399338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense variant
orthologous variants: 71659965-G-C

215399361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659982-A-G

http://identifiers.org/hco/2/GRCh38#215399364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71659985-A-C

215399364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71659985-A-G

215399381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71660005-A-G

http://identifiers.org/hco/2/GRCh38#215399421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71660045-A-C

215399488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71660113-G-A

215399488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71660113-G-T

215400379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71660417-T-A

215400379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71660417-T-C

215402261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71660849-G-T

215402448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71661036-C-T

215403032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71661355-C-T

215403372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71661695-A-G

215403521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71661948-G-A

215403618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71662040-A-G

215403767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71662188-A-T

215404133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71662996-T-C

215404179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663027-C-T

215404224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663070-A-G

215404250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663095-G-C

215404250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663095-G-T

http://identifiers.org/hco/2/GRCh38#215404265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71663110-A-C

215404265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663110-A-G

215404354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663182-T-A

215404354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663182-T-C

215404406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense variant
orthologous variants: 71663254-G-A

215404406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense variant
orthologous variants: 71663254-G-T

215404514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense variant
orthologous variants: 71663362-T-G

215404670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663522-G-T

215404697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663549-G-A

215404697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663549-G-T

215404735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663586-G-T

http://identifiers.org/hco/2/GRCh38#215404791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71663643-A-C

215404795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663647-A-T

215405032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71663894-T-C

215405869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71664468-T-C

215405869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71664468-T-G

215405883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71664482-T-C

http://identifiers.org/hco/2/GRCh38#215406110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71664995-C-A

215406110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71664995-C-T

215406120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71665003-G-A

215406120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71665003-G-T

215406131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71665014-T-C

215406179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71665063-A-T

215406184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71665068-C-T

215406196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71665079-G-T

215406467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71665362-T-C

http://identifiers.org/hco/2/GRCh38#215406503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71665398-C-A

215406503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71665398-C-T

215406506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71665401-T-C

215406682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71665615-A-G

215407017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71666011-T-C

http://identifiers.org/hco/2/GRCh38#215407059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71666146-C-A

215407080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71666192-A-G

215407368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71666563-A-G

215407452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71666622-T-C

http://identifiers.org/hco/2/GRCh38#215407457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71666627-C-A

215407680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71666833-T-G

215407750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71666869-G-A

215407790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71666902-C-T

http://identifiers.org/hco/2/GRCh38#215407892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71667001-A-C

215407901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667008-G-C

215407944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667050-C-T

215407952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667077-C-G

215407952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667077-C-T

http://identifiers.org/hco/2/GRCh38#215407968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71667094-A-C

215407968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667094-A-G

215407968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667094-A-T

http://identifiers.org/hco/2/GRCh38#215407978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71667104-A-C

215408006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667133-G-T

http://identifiers.org/hco/2/GRCh38#215408032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71667155-C-A

215408032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667155-C-T

215408033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667156-A-G

215408034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667157-G-A

215408034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667157-G-T

http://identifiers.org/hco/2/GRCh38#215408053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71667176-C-A

215408053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71667176-C-G

http://identifiers.org/hco/2/GRCh38#215408063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71667185-C-A

http://identifiers.org/hco/2/GRCh38#215408457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71667726-A-C

215408534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667781-C-T

215408535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667782-G-A

215408535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667782-G-C

215408535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71667782-G-T

215409111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668112-T-C

215409213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668185-A-G

215409443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668382-G-T

215409460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668399-G-C

215409460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668399-G-T

215409468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668408-C-T

215409510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668450-A-G

215409560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71668472-T-A

http://identifiers.org/hco/2/GRCh38#215409591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71668503-A-C

215409591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71668503-A-G

215409630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71668542-G-A

http://identifiers.org/hco/2/GRCh38#215409633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71668545-A-C

215409714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71668626-A-G

215409726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71668638-T-C

215409762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71668675-A-G

215409918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71668809-G-A

215409918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71668809-G-C

215409926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 71668817-G-A

215409992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71668880-G-T

215410178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71669027-G-A

215410178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71669027-G-T

215410911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71669361-A-G

215410980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71669427-C-G

215411048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71669512-G-A

215411136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71669597-A-G

215411341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71669810-T-G

215411456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71669928-G-A

http://identifiers.org/hco/2/GRCh38#215414196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71670596-A-C

http://identifiers.org/hco/2/GRCh38#215414419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71670800-A-C

215414536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71670920-T-A

http://identifiers.org/hco/2/GRCh38#215414632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71670993-C-A

215414717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71671076-G-A

215414717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71671076-G-T

215414726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71671085-A-G

215414783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71671148-G-C

215414783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71671148-G-T

215414789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 71671155-A-G

215414807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 71671171-G-C

215415016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671367-A-T

215415036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671390-T-C

215415060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671413-G-A

215415060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671413-G-T

215415067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671420-G-C

215415067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671420-G-T

215415128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671474-G-A

215415134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671481-C-T

215415212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671549-T-A

215415213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671550-A-T

215415266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671609-G-A

215415582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71671919-T-G

215415948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71672250-C-T

215416022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71672324-G-C

215416118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71672411-A-G

215416585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71672817-T-G

215416635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71672867-T-C

215416897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71673086-G-A

215417352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71673705-A-T

215418797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71675809-C-G

215418815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71675829-C-T

215418830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71675842-C-T

215418862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71675874-T-C

215418872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71675884-C-G

215418949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71675996-A-T

215419072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71676265-G-C

215419112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71676304-A-G

215419112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71676304-A-T

215419394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676563-C-T

215419433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676602-T-A

215419433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676602-T-C

215419459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676616-G-A

215419459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676616-G-T

215419655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71676904-A-G

215419825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71677060-T-A

215420773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71677716-G-A

215420773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 71677716-G-C

215420773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 71677716-G-T

http://identifiers.org/hco/2/GRCh38#215420788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#71677731-A-C

215420810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71677753-G-A

215421014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71677941-G-T

http://identifiers.org/hco/2/GRCh38#215421105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71678031-C-A

215421236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678155-G-A

215421236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678155-G-T

215421259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71678628-A-G

215421282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71678651-G-T

215421340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71678711-T-C

215421379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71678749-G-C

215421379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71678749-G-T

215421401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71678775-T-C

215421454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71678830-C-T

http://identifiers.org/hco/2/GRCh38#215421697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71679074-A-C

215421954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71679351-G-T

215421960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71679357-T-C

215421961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71679358-A-G

215421983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679380-T-C

215421999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679396-T-G

http://identifiers.org/hco/2/GRCh38#215422040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71679426-C-A

215422040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679426-C-G

215422072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, undefined
orthologous variants: 71679432-T-C

215422191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71679551-A-G

215422268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679626-C-G

215422268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679626-C-T

215422280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679638-G-T

215422282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679640-T-A

215422282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679640-T-C

215422303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679661-G-A

215422303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679661-G-C

215422303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679661-G-T

215422304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679662-T-C

http://identifiers.org/hco/2/GRCh38#215422360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71679722-C-A

215422360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679722-C-T

215422367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679729-T-A

215422367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679729-T-G

215422451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679791-T-C

215422476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679816-G-C

215422604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71679931-T-C

215422785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71680101-G-C

215422841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71680154-C-T

215422868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71680164-T-G

215423381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71680342-G-A

215423602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71680567-G-A

215423602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71680567-G-T

http://identifiers.org/hco/2/GRCh38#215423623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71680588-C-A

215423623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71680588-C-T

215423638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71680603-T-A

http://identifiers.org/hco/2/GRCh38#215423656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71680622-A-C

215423656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71680622-A-T

215423966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71680934-C-T

http://identifiers.org/hco/2/GRCh38#215424021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71680983-C-A

215424062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681023-T-A

http://identifiers.org/hco/2/GRCh38#215424077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71681037-C-A

215424104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681076-T-G

http://identifiers.org/hco/2/GRCh38#215424115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71681081-C-A

215424115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681081-C-T

215424137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681102-G-A

215424255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71681220-C-T

215424364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681327-G-T

215424413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681379-G-A

215424447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681414-T-A

215424447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681414-T-C

215424543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681459-T-C

215424563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681479-C-T

215424751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681644-A-G

215424766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71681654-G-A

215425005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71682026-G-T

215425006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71682027-T-G

215425022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71682052-T-G

215425075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71682100-T-C

215425215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71682240-A-G

215425329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71682355-G-A

215427170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71683290-T-C

http://identifiers.org/hco/2/GRCh38#215427266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71683397-A-C

215427266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71683397-A-G

215427421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71683550-G-A

215428040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71684624-A-G

215428053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71684635-T-A

215428407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71684931-A-G

215428435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71684965-A-G

215428488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71685019-T-C

215429516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71686507-C-T

215429749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71686329-T-C

215429751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71686327-C-T

http://identifiers.org/hco/2/GRCh38#215430103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71685834-A-C

215430117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71685820-G-C

215430220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71685725-A-T

215430276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71685671-A-G

215430294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71685649-A-G

215430573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71687053-T-A

215430573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71687053-T-C

215430679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71687132-C-G

215430683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71687136-C-T

http://identifiers.org/hco/2/GRCh38#215430812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71687265-C-A

215430887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71687343-A-G

http://identifiers.org/hco/2/GRCh38#215430905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71687361-C-A

215430905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71687361-C-T

215431285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71687831-A-G

215431382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71687909-G-A

215431382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71687909-G-C

215431419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71687984-G-T

215431616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688179-C-T

215431631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688194-T-C

215431683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688242-T-C

215431683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688242-T-G

215431715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688257-A-G

215431744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688284-G-T

215431773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688316-G-C

215431773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688316-G-T

215431810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688330-G-A

http://identifiers.org/hco/2/GRCh38#215431821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71688341-A-C

215431878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense variant
orthologous variants: 71688398-C-T

215431954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense variant
orthologous variants: 71688474-A-T

215431986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688506-T-C

215431997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688518-G-A

215432051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688574-G-A

215432051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688574-G-T

215432219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688760-A-G

215432476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71688983-C-T

215432654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71689145-A-T

215432718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71689207-T-G

215433178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71689585-G-T

215433212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71689615-C-G

215433248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71689646-C-G

215433260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71689658-G-A

215433260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71689658-G-T

215433300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71689697-C-T

215433468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71689872-G-A

215433468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71689872-G-C

215433481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71689885-C-G

215433483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71689887-A-G

215433839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71690143-C-T

215433964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71690156-T-G

215434240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71690245-A-T

215434784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71690768-T-C

215434831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 71690815-A-T

215434911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71690999-A-G

215434911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71690999-A-T

215434954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71691059-T-C

215434955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71691060-G-A

215434955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71691060-G-T

215434964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71691069-A-G

215435168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71691509-T-A

215435538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71691858-A-G

215435538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71691858-A-T

215435636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71691971-G-A

215435636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: intron variant
orthologous variants: 71691971-G-T

215435677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71692013-C-G

215435677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71692013-C-T

215435686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71692022-G-A

215435686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: synonymous variant
orthologous variants: 71692022-G-C

215435726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense variant
orthologous variants: 71692062-G-A

215435726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense variant
orthologous variants: 71692062-G-T

215435747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: missense variant
orthologous variants: 71692083-G-A

http://identifiers.org/hco/2/GRCh38#215436045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#71692308-C-A

215436045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 5 prime UTR variant
orthologous variants: 71692308-C-G

215436045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 5 prime UTR variant
orthologous variants: 71692308-C-T

215436071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 5 prime UTR variant
orthologous variants: 71692334-C-G

215436071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3778
most severe consequence: 5 prime UTR variant
orthologous variants: 71692334-C-T