46330259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77657287-A-G

46330263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77657283-T-C

http://identifiers.org/hco/18/GRCh38#46330338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77657212-A-C

46330375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77656848-T-C

http://identifiers.org/hco/18/GRCh38#46330521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77656727-A-C

46330521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77656727-A-T

46330522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77656726-A-G

46330524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77656716-C-G

46330667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77656566-G-C

46330813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77656425-A-T

46330896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77656355-C-T

46331613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77655675-T-A

46331859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77655455-C-T

46333172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77653823-A-G

46333185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77653810-G-A

46333185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77653810-G-T

46333297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77653704-T-C

46333675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron_variant, undefined
orthologous variants: 77653341-C-G

46333852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77653196-T-G

46333875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77653177-T-C

46333875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77653177-T-G

46333918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: intron variant
orthologous variants: 77653129-T-G

http://identifiers.org/hco/18/GRCh38#46334170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77652886-C-A

46334170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77652886-C-T

46334206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77652859-G-A

46334206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77652859-G-C

http://identifiers.org/hco/18/GRCh38#46334207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77652858-C-A

46334207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77652858-C-G

46334207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77652858-C-T

46334452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77652602-G-A

46334452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 77652602-G-T

http://identifiers.org/hco/18/GRCh38#46334671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77652378-C-A

46334671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652378-C-T

46334711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652338-T-A

46334711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652338-T-C

46334713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652336-T-A

46334713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652336-T-C

46334806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652236-T-A

46334806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652236-T-C

46334806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652236-T-G

46334840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652202-G-A

46334840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652202-G-C

46334840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652202-G-T

http://identifiers.org/hco/18/GRCh38#46334943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77652102-A-C

http://identifiers.org/hco/18/GRCh38#46334955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77652089-C-A

46334955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77652089-C-T

46335054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77651983-G-A

46335054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77651983-G-T

46335331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77651699-T-C

46335377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77651653-T-C

http://identifiers.org/hco/18/GRCh38#46335571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77651478-C-A

46335571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77651478-C-G

46335571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77651478-C-T

http://identifiers.org/hco/18/GRCh38#46335578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77651471-C-A

46335578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77651471-C-G

46335578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77651471-C-T

http://identifiers.org/hco/18/GRCh38#46336026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77651005-C-A

http://identifiers.org/hco/18/GRCh38#46336114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77650943-C-A

46336114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77650943-C-T

46336238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77650818-A-T

46336412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77650652-G-A

46336412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77650652-G-T

46336499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77650558-C-G

46336499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77650558-C-T

46336501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77650556-C-G

46336501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77650556-C-T

46336812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77650247-G-A

46337238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77649819-A-G

http://identifiers.org/hco/18/GRCh38#46337748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77649205-C-A

46337748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77649205-C-T

46337757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77649196-C-G

46337773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77649179-G-A

46337773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77649179-G-C

46337773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77649179-G-T

46337854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77649061-C-T

46338206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77648715-G-C

46338219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77648702-T-C

46338219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77648702-T-G

46338747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77648170-G-A

46338747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77648170-G-C

46338768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77648148-T-C

46339266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77647653-T-C

46339266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77647653-T-G

http://identifiers.org/hco/18/GRCh38#46339752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77647175-C-A

46339753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77647174-C-T

46339760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77647167-C-T

46341056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77646101-G-A

46341501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77645809-A-G

46341577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77645748-T-C

46341851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77645518-T-G

46342122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77645185-C-T

46342431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77644915-G-A

46342553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77644833-G-A

46342807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77644641-T-A

46342905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77644516-G-A

46343342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77644034-A-G

46343342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77644034-A-T

46343367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77644008-A-G

46343686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77643741-G-A

46344030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77643554-C-T

46344035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77643549-G-T

46344041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77643543-A-T

46344085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77643507-A-G

46344100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77643491-G-A

http://identifiers.org/hco/18/GRCh38#46344196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#77643427-A-C

http://identifiers.org/hco/18/GRCh38#46344785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77642861-C-A

46345014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77642682-A-T

46345110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77642642-T-G

46345330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77642496-G-A

46345330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77642496-G-C

46345349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77642490-G-T

46345469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77642346-C-T

http://identifiers.org/hco/18/GRCh38#46345590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77642208-A-C

46345607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77642191-C-T

46346193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77641814-G-C

46346193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77641814-G-T

46346433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77641612-C-T

46346495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77641533-G-T

46346656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77641307-A-G

46346658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77641305-T-C

46346658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77641305-T-G

46346671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77641295-A-G

46346758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77641208-C-T

46346823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77641145-A-G

http://identifiers.org/hco/18/GRCh38#46347379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77640615-C-A

46347739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77640318-G-A

46347842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77640227-G-C

46348013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77640095-C-T

46348069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77640042-G-A

46348069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77640042-G-T

46348333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77639851-G-T

46348743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77639459-T-C

46348958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77639247-A-G

46349032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77639181-A-G

46350174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77638757-C-G

46350265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77638652-G-A

46350280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77638640-C-T

46350432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77638431-A-G

46350533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77638336-C-T

46353316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77637082-T-C

46353531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77636927-G-A

46353596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77636887-C-T

http://identifiers.org/hco/18/GRCh38#46353797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77636691-C-A

46353885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77636589-G-A

46353974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77636524-C-T

46354087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77636407-G-T

46354095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77636399-A-G

46354131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77636361-G-C

46354858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77635286-G-A

46355533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77634923-T-C

46355555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77634901-G-A

46355690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77634768-T-C

46355886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77634578-C-T

46356094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77634393-A-T

46356293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77634164-C-T

46356363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77634113-T-A

46356406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77634070-G-C

46356406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77634070-G-T

46356419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77634057-T-G

46356708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77633396-C-T

46356709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77633395-C-T

46356729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77633376-C-T

46356771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77633334-G-A

46356805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77633302-A-G

46357371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77633018-G-T

46357776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77632641-G-A

46357842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77632609-C-T

46358111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77632342-G-A

46358225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77632222-A-G

46358328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77632138-G-A

46358445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77632026-G-A

46358486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77631986-C-T

46358568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77631808-A-G

46358572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77631804-C-T

46358596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77631769-G-C

46358597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77631768-G-A

46358678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77631689-G-A

46358693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77631677-G-A

46358693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77631677-G-T

http://identifiers.org/hco/18/GRCh38#46358702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77631668-C-A

46358939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77631445-C-T

46359006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77631396-T-G

46359604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77630873-A-G

46359745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77630728-C-T

46359810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77630664-C-G

46360400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77630176-A-G

46360508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77630068-G-A

46360615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77629953-C-T

46360629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77629939-C-T

46360755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77629837-C-T

46360761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77629831-G-A

46360816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77629790-G-T

46361340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77629284-A-G

46361522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77629134-G-A

46361522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77629134-G-T

46362657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77628133-C-T

46362658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77628132-C-T

46366756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77627877-G-A

46366781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77627852-C-T

46366897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77627739-C-G

46367700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77626975-G-A

46367700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77626975-G-T

46368437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77625309-G-C

46368465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77625281-T-A

46368465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77625281-T-C

46368482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77625262-G-T

46368519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77625226-G-A

46369181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77624967-C-T

46369393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77624733-G-C

46369393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77624733-G-T

46369541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77624584-G-A

46369575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77624550-C-T

46369948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77624285-C-G

46369948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77624285-C-T

46369949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77624284-G-A

http://identifiers.org/hco/18/GRCh38#46369968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77624244-C-A

46369968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77624244-C-T

46369988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77624224-G-T

46370051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77624161-A-G

46370443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77623800-A-T

46370507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77623748-T-C

46370639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77623644-G-A

http://identifiers.org/hco/18/GRCh38#46370655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77623620-C-A

46371679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77623127-G-T

46371747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77623044-G-C

46371806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77623004-G-A

46371970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77622808-G-A

46372025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77622749-T-A

46372338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77622486-G-A

46372453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77622372-G-C

46372506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77622351-A-T

46372577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77622298-G-A

46372715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77622160-G-A

46372979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621947-C-T

46373016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621910-A-G

46373151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621545-G-A

46373151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621545-G-T

46373246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621461-G-T

46373415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621320-G-A

http://identifiers.org/hco/18/GRCh38#46373611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77621137-A-C

46373640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621111-C-T

46373642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621109-C-T

46373646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621093-G-A

46373656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621083-G-A

46373666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77621069-C-G

46373795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620959-A-G

46373799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620955-C-T

46373817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620954-G-T

46373827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620947-G-A

46373944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620850-C-G

46373944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620850-C-T

46373999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620797-C-T

46374141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620663-T-A

http://identifiers.org/hco/18/GRCh38#46374579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77620296-C-A

46374718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620262-C-T

46374719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620261-G-A

http://identifiers.org/hco/18/GRCh38#46374735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77620247-C-A

46374735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620247-C-T

46375027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77620050-G-T

http://identifiers.org/hco/18/GRCh38#46375090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77619987-C-A

46375214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619889-G-A

46375220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619883-A-G

http://identifiers.org/hco/18/GRCh38#46375723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77619715-C-A

46375757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619681-G-A

http://identifiers.org/hco/18/GRCh38#46375893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77619559-A-C

46375893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619559-A-G

46375893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619559-A-T

46375920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619532-G-A

46376057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619401-G-A

46376107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619353-C-T

46376152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619313-G-A

46376247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619235-G-A

46376343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619177-G-A

46376349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77619171-A-G

46376750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77618096-A-G

46377073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617944-C-T

46377194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617821-T-C

46377194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617821-T-G

46377652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617466-A-G

46377669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617443-G-A

46377688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617424-G-A

46377688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617424-G-C

46377688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617424-G-T

46377962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617181-T-C

46378084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617101-G-T

46378120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617065-A-G

http://identifiers.org/hco/18/GRCh38#46378687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77617300-A-C

http://identifiers.org/hco/18/GRCh38#46378700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77617287-C-A

46378710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77617277-T-C

46378897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77615584-C-T

46379189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77615394-G-A

46379189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77615394-G-T

46379539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77615129-C-T

46379793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77615017-T-A

46379799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77615011-T-C

46379820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77614990-C-G

46380044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77614785-T-A

46380056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77614770-T-A

46380056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77614770-T-G

46380186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77614647-A-G

46380425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77614421-T-C

46380472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77614360-G-T

46380477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77614355-T-G

http://identifiers.org/hco/18/GRCh38#46380480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77614352-A-C

46380480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77614352-A-G

46380643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77614209-T-C

46381206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77613320-C-T

46381271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77613263-T-C

46381283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77613251-G-C

46381308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77613226-G-A

46381431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77613108-C-G

46381433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77613106-A-G

46383004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77612518-G-T

46383032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77612490-G-A

46383211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77612343-G-T

http://identifiers.org/hco/18/GRCh38#46383387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77612173-C-A

46383387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77612173-C-T

http://identifiers.org/hco/18/GRCh38#46383454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77612112-A-C

46383454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77612112-A-G

46383456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77612110-G-A

46384361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77611677-G-A

http://identifiers.org/hco/18/GRCh38#46384467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77611619-C-A

46384467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77611619-C-T

46384495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77611591-G-A

46385268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77611041-C-T

46385368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77610888-G-A

http://identifiers.org/hco/18/GRCh38#46385399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77610851-C-A

46385399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77610851-C-T

46385408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77610842-A-G

http://identifiers.org/hco/18/GRCh38#46385757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77610569-C-A

46385757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77610569-C-G

46385757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77610569-C-T

46385781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77610545-T-C

46385805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77610521-G-C

http://identifiers.org/hco/18/GRCh38#46385985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77610344-A-C

http://identifiers.org/hco/18/GRCh38#46385989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77610340-C-A

46386103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77610227-T-C

46386119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77610212-T-C

46386145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77610179-G-A

46386314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77610041-C-T

46386333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77610023-G-T

http://identifiers.org/hco/18/GRCh38#46386338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77610018-C-A

46386339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77610017-C-T

http://identifiers.org/hco/18/GRCh38#46386475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77609887-C-A

46386475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609887-C-T

http://identifiers.org/hco/18/GRCh38#46386486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77609876-C-A

46386486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609876-C-T

46386532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609659-T-C

http://identifiers.org/hco/18/GRCh38#46386541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77609650-C-A

46386541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609650-C-G

46386541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609650-C-T

http://identifiers.org/hco/18/GRCh38#46386562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77609621-C-A

http://identifiers.org/hco/18/GRCh38#46386599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77609504-A-C

46386599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609504-A-G

46386608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609422-G-A

46386753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609293-A-G

46386758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609288-G-A

46386768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609278-G-A

46386768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609278-G-T

46386900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609156-T-A

46386903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609153-T-C

46386923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609136-G-A

46386923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609136-G-T

46386943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609116-G-T

46386977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609087-G-A

46386977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77609087-G-T

http://identifiers.org/hco/18/GRCh38#46387195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77608912-C-A

http://identifiers.org/hco/18/GRCh38#46387207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77608897-C-A

46387207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77608897-C-G

46387207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77608897-C-T

46387219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77608885-G-T

http://identifiers.org/hco/18/GRCh38#46387220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77608884-C-A

http://identifiers.org/hco/18/GRCh38#46387257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77608852-C-A

46387257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77608852-C-T

http://identifiers.org/hco/18/GRCh38#46388016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77608616-C-A

46388016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77608616-C-T

46388017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77608615-G-A

46388017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77608615-G-T

46388096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77608534-G-A

46388096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77608534-G-C

46388163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77608490-T-G

46388529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77608208-T-G

46388595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77608146-A-G

46388628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77608113-T-A

46388910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77607805-C-G

46388910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77607805-C-T

46389056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77607658-G-A

46389082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77607630-A-G

http://identifiers.org/hco/18/GRCh38#46389094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77607618-C-A

46389463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77607269-G-T

http://identifiers.org/hco/18/GRCh38#46389516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: -C-A

46389516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: -C-T

46389538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77607205-T-C

46389584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77607159-C-T

http://identifiers.org/hco/18/GRCh38#46389621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77607133-C-A

46389658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77607093-G-A

46389696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77607053-T-C

46390224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77606869-T-A

46390249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77606845-G-A

http://identifiers.org/hco/18/GRCh38#46390259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77606831-C-A

46390504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77606509-C-T

46390841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77606119-G-A

46390841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77606119-G-T

46392242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77605602-A-G

46392420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77605441-G-A

46392420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77605441-G-T

46392492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77605358-C-T

46392559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77605292-T-C

46392566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77605285-G-A

46392629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77605220-C-T

46392840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77605091-G-C

46392875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77605065-G-C

46393082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77604901-C-T

46393478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77604401-G-A

46393478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77604401-G-T

46393511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77604368-A-G

46393513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77604366-C-G

46393513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77604366-C-T

http://identifiers.org/hco/18/GRCh38#46394115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77603461-C-A

46394123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77603453-C-T

46394124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77603452-T-C

46394160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77603409-G-C

46394160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77603409-G-T

46394505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77603077-C-G

46394505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77603077-C-T

http://identifiers.org/hco/18/GRCh38#46394571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77603028-C-A

46394627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77602973-C-G

46394756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77602865-C-G

46394756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77602865-C-T

46395096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77602575-C-T

46395875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77600798-C-T

46396250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77600438-A-G

46396388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77600309-G-A

46396547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77600147-A-G

46396597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77600081-T-G

46396863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77599847-C-T

46397074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77599617-A-G

46397075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77599616-G-C

46397134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77599571-G-A

46397201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77599521-G-A

46397221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77599500-T-C

46397517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77599104-G-A

46397517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77599104-G-C

46397538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77599083-G-T

46397589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77599036-T-C

46397589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77599036-T-G

46398455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77598852-C-T

46398589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77598718-A-T

46398969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77598439-G-C

46399018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77598393-C-G

46399391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77598021-C-G

http://identifiers.org/hco/18/GRCh38#46399435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77597986-C-A

46399454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77597967-C-T

46399942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77597463-A-T

46403226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596800-G-A

46403226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596800-G-T

46403266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596760-G-A

46403437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596641-A-G

46403515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596560-T-C

46403517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596558-C-G

46403517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596558-C-T

46403738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596509-C-T

46404109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596288-C-G

46404123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596275-G-A

46404304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77596117-T-G

46404856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77595979-G-A

46404946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77595901-C-T

http://identifiers.org/hco/18/GRCh38#46404950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77595895-C-A

46405060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77595776-G-T

46405204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77595650-G-C

46405292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77595587-C-T

http://identifiers.org/hco/18/GRCh38#46405971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77594623-C-A

46405971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77594623-C-T

46406357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77594280-T-C

46406538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77594103-T-A

46406538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77594103-T-C

http://identifiers.org/hco/18/GRCh38#46406552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77594087-C-A

46406552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77594087-C-T

46406727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77593934-C-T

46406812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77593855-C-G

46406821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77593846-T-A

46406821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77593846-T-C

http://identifiers.org/hco/18/GRCh38#46406871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77593797-C-A

46406871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77593797-C-T

46406927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77593760-G-A

46407330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77593376-C-G

46407967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77592715-C-G

46408356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77592553-C-T

46408411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77592485-C-T

46409894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77592054-C-T

46410150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77591843-C-T

46410223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77591782-C-G

http://identifiers.org/hco/18/GRCh38#46410227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77591778-C-A

http://identifiers.org/hco/18/GRCh38#46410252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77591764-A-C

46410332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77591709-A-G

46410454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77591531-T-A

46410485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 77591502-A-T

http://identifiers.org/hco/18/GRCh38#46410690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77591298-C-A

46410821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77591198-C-T

46410928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77591082-C-T

46410986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77591008-C-T

46411269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77590750-G-A

46411269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77590750-G-C

46411280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77590739-G-A

http://identifiers.org/hco/18/GRCh38#46411554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77590099-C-A

46411567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77590086-G-A

46411585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77590077-G-A

46412271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77589416-G-C

46412350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77589320-C-T

46412379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77589292-C-T

http://identifiers.org/hco/18/GRCh38#46412383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77589288-C-A

46412551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77589121-C-T

46412577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77589114-C-G

46412577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77589114-C-T

46412592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77589100-G-A

46413282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77588516-C-G

46413282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77588516-C-T

46413642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77587922-C-T

46413666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77587816-A-T

46413811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77587683-T-C

46414878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77586875-T-C

46415748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77586442-A-G

46415849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77586380-G-T

46415881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77586348-G-A

46415897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77586332-C-T

46415907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77586321-G-A

46416422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77585069-T-A

46416422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77585069-T-C

46416497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77584993-A-G

46416649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77584901-G-C

46416666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77584884-A-G

46418699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77583961-A-G

http://identifiers.org/hco/18/GRCh38#46418768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77583896-C-A

46418849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77583833-T-C

46419019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77583700-C-T

46419062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77583661-C-T

46419238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77583570-G-T

46419404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77583443-G-T

46419580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77583274-C-T

46419792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77583070-C-G

46419792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77583070-C-T

http://identifiers.org/hco/18/GRCh38#46419841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77583003-C-A

46419841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77583003-C-G

46419841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77583003-C-T

46419977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77582792-A-G

http://identifiers.org/hco/18/GRCh38#46420152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77582622-A-C

46420275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77582555-G-A

46420379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77582476-C-T

46420407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77582446-G-A

46421329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581672-G-T

46421410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581596-G-A

http://identifiers.org/hco/18/GRCh38#46421466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77581542-C-A

46421466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581542-C-T

46421502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581518-T-C

http://identifiers.org/hco/18/GRCh38#46421555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77581460-C-A

46421555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581460-C-G

46421578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581437-G-A

46421722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581340-G-T

46421784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581281-T-C

46421901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581143-G-A

46422005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581048-A-G

46422009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581044-C-T

46422016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581037-A-T

46422048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77581005-T-C

46422068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77580985-G-A

46422284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77580825-T-G

46422762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77580409-C-T

46422763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77580408-C-T

46422842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77580354-T-C

http://identifiers.org/hco/18/GRCh38#46422895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77580266-C-A

46422991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 77580186-G-A

46423039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77580142-C-G

46423329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77579903-G-T

46423346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77579885-C-T

46423446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77579793-T-C

46423678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77579540-A-G

46424029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578994-G-T

46424033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578990-G-C

46424044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578979-C-T

46424084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578883-A-G

46424084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578883-A-T

46424354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578657-G-A

46424495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578556-A-G

46424719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578344-C-T

46424745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578322-C-T

http://identifiers.org/hco/18/GRCh38#46424834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77578270-C-A

46424850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578265-T-A

46424854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578261-G-T

46424995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578135-T-C

46425010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578122-T-C

46425090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578057-T-C

46425136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77578011-T-C

46425343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77577786-T-G

46425881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77577142-C-G

46425935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77577076-C-T

46426174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77576877-A-G

46426555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77576451-C-T

46427276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77575803-C-T

46427317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77575762-G-A

http://identifiers.org/hco/18/GRCh38#46427325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77575761-C-A

46427588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77575597-A-G

46427638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77575547-A-T

46428485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77575396-G-A

46428485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77575396-G-C

46428485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77575396-G-T

46428567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77575311-T-C

46428779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77575161-A-G

http://identifiers.org/hco/18/GRCh38#46428801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77575141-C-A

46429498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77574596-T-C

http://identifiers.org/hco/18/GRCh38#46429568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77574537-A-C

46429653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77574462-T-A

46431554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77573508-G-T

46432361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77572861-T-G

46432756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77572546-G-A

46432901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77572418-C-T

http://identifiers.org/hco/18/GRCh38#46433123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77572224-C-A

46433123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77572224-C-T

46433136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77572211-G-A

46433136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77572211-G-T

http://identifiers.org/hco/18/GRCh38#46433152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77572195-C-A

46433152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77572195-C-T

http://identifiers.org/hco/18/GRCh38#46433160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77572187-C-A

46433379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 77571969-C-G

46433563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77571810-G-A

http://identifiers.org/hco/18/GRCh38#46433564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77571809-C-A

46433564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77571809-C-G

46433564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77571809-C-T

http://identifiers.org/hco/18/GRCh38#46433621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77571799-C-A

46433621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77571799-C-T

46433651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77571789-C-G

46433651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77571789-C-T

46434165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77571375-A-G

46434225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77571309-C-T

46434665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563664-G-A

46434714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563631-C-T

46434856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563501-G-A

46435172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563387-G-A

46435172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563387-G-T

46435209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563355-G-A

46435209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563355-G-T

http://identifiers.org/hco/18/GRCh38#46435226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77563342-C-A

46435230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563338-T-G

46435269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563297-C-G

46435269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563297-C-T

46435409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563155-G-C

46435409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563155-G-T

46435420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563086-G-A

46435420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563086-G-T

46435426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563080-G-A

46435428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563078-G-A

46435428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563078-G-C

46435428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563078-G-T

46435436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563070-G-C

http://identifiers.org/hco/18/GRCh38#46435456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77563050-C-A

46435456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563050-C-T

46435495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563010-G-T

46435497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563008-G-A

46435497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77563008-G-T

http://identifiers.org/hco/18/GRCh38#46435597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77562927-A-C

46436608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77562383-A-G

46436686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77562301-C-T

46436978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77562011-C-T

46437102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77561887-C-T

46437278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77561755-G-A

46437278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 77561755-G-C

46444866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77559276-T-C

46444944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77559220-C-G

46445012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77559131-T-A

46445796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77558173-A-T

46445807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77558162-T-G

46445934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77557953-G-A

46446107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77557659-G-A

46446272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77557508-A-T

46446399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77557378-G-A

46446479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77557323-T-C

46446626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77557225-G-A

46446797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77557089-T-G

46446868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77557016-A-G

46447151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77556556-C-T

46447237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77556475-C-G

http://identifiers.org/hco/18/GRCh38#46447360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77556337-C-A

46447360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77556337-C-T

46447436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77556224-T-A

46447436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77556224-T-C

46447450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77556210-G-A

46447450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77556210-G-T

46447455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77556206-G-A

http://identifiers.org/hco/18/GRCh38#46447481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77556176-C-A

46447481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77556176-C-T

46447488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77556155-T-G

http://identifiers.org/hco/18/GRCh38#46447495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77556148-C-A

46447497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77556146-G-A

46447547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77556080-G-A

46447678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77555949-T-G

46447684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77555943-A-G

46447684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77555943-A-T

46447706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77555914-G-A

46447755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77555883-G-A

46447755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77555883-G-C

46447755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77555883-G-T

46447791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77555844-C-T

46447796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77555839-T-C

46449905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77555129-T-A

46450026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77555009-G-A

46450050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554998-T-G

46450089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554945-T-C

46450212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554822-G-A

46450217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554817-A-T

46450220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554814-G-C

46450220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554814-G-T

http://identifiers.org/hco/18/GRCh38#46450625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77554539-C-A

46450625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554539-C-T

46450674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554495-G-A

46450710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77554460-C-G

46450755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77554415-C-G

46450820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554352-G-A

http://identifiers.org/hco/18/GRCh38#46450822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77554350-C-A

http://identifiers.org/hco/18/GRCh38#46450879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77554287-C-A

46450879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554287-C-T

46450885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554282-G-A

46450885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554282-G-C

46450885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554282-G-T

http://identifiers.org/hco/18/GRCh38#46450895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77554272-C-A

46450895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554272-C-T

46450967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554200-T-C

46451037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77554129-G-A

46451182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77553993-G-A

46451182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77553993-G-T

http://identifiers.org/hco/18/GRCh38#46451288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77553910-C-A

46451293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77553905-G-A

46451498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77553740-A-G

46454341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77551988-C-T

46454425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77551903-A-G

46454477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77551861-A-G

46454705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77551663-C-T

46454764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 77551603-G-C

46456010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 77550648-G-A

46456162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77550475-G-T

46456252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77550387-G-T

46456282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77550357-A-T

46456403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77550257-G-T

http://identifiers.org/hco/18/GRCh38#46456404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77550256-C-A

46456404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77550256-C-T

http://identifiers.org/hco/18/GRCh38#46456407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77550253-C-A

46456407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77550253-C-T

46456447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77550193-G-C

46456485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77550178-T-A

http://identifiers.org/hco/18/GRCh38#46456487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77550176-C-A

46456487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 77550176-C-T

http://identifiers.org/hco/18/GRCh38#46456492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77550171-C-A

46456785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549864-G-A

46456785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549864-G-T

46456809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549837-G-A

46456809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549837-G-C

46456811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549835-G-T

46456862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549786-G-T

http://identifiers.org/hco/18/GRCh38#46456883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77549765-C-A

46456883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549765-C-T

46456894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549754-G-T

46456895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549753-G-T

46456905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549743-G-T

46456988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549662-T-C

http://identifiers.org/hco/18/GRCh38#46457096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77549555-C-A

46457096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549555-C-G

46457096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549555-C-T

http://identifiers.org/hco/18/GRCh38#46457178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77549474-C-A

46457338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549254-T-C

46457437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549168-G-A

46457437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77549168-G-T

46457741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548842-G-T

http://identifiers.org/hco/18/GRCh38#46457742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77548841-A-C

46457742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548841-A-G

46457742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548841-A-T

46457747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548836-G-A

http://identifiers.org/hco/18/GRCh38#46457769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77548814-C-A

46457769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548814-C-T

46457775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548808-G-A

http://identifiers.org/hco/18/GRCh38#46457830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77548755-C-A

46457832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548753-T-C

46457838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548748-A-G

46457890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548702-G-T

46458067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548553-G-T

46458086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548534-T-C

46458108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548510-G-A

46458108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548510-G-C

46458163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548453-G-T

46458285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548353-G-C

46458285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548353-G-T

http://identifiers.org/hco/18/GRCh38#46458306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77548331-C-A

46458306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548331-C-T

46458330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548310-T-C

46458349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548291-T-G

46458392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548202-G-A

46458392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548202-G-C

46458392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548202-G-T

46458413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548173-T-A

46458413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548173-T-C

46458472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548131-A-G

http://identifiers.org/hco/18/GRCh38#46458533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77548072-A-C

46458533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548072-A-G

46458621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77548003-T-C

46458790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77547870-A-G

46459034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77547655-T-C

http://identifiers.org/hco/18/GRCh38#46459053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77547636-C-A

http://identifiers.org/hco/18/GRCh38#46459271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77547414-C-A

46459271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77547414-C-T

46459295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77547390-A-G

46459295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77547390-A-T

46459403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77547271-C-T

http://identifiers.org/hco/18/GRCh38#46459440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77547236-C-A

46459440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77547236-C-T

46459631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77547066-C-T

46459756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546951-A-G

46459757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546950-G-T

46459768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546939-G-A

46459768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546939-G-T

46459777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546930-G-T

46459800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546907-A-G

46460111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546631-T-A

46460230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546519-A-G

http://identifiers.org/hco/18/GRCh38#46460241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77546508-C-A

46460241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546508-C-T

46460247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546498-G-A

46460247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77546498-G-T

http://identifiers.org/hco/18/GRCh38#46460984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77545759-C-A

46460984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545759-C-T

46461021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545730-A-G

46461039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545721-C-T

46461086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545664-G-C

46461087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545663-G-T

46461118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545636-T-C

46461172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545605-A-G

46461201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545594-G-T

46461207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545588-T-G

46461294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545502-A-G

46461686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545128-G-A

46461686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545128-G-T

46461764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545041-T-C

46461766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545039-G-A

46461809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545006-G-C

46461809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77545006-G-T

46461888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544925-G-T

http://identifiers.org/hco/18/GRCh38#46461938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77544909-C-A

46461946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544901-T-C

46461964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544885-A-G

46461971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544878-T-G

http://identifiers.org/hco/18/GRCh38#46462066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77544784-C-A

46462066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544784-C-T

http://identifiers.org/hco/18/GRCh38#46462098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77544761-C-A

46462113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544746-A-G

46462401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544508-G-A

46462401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544508-G-T

46462404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544505-C-G

46462404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544505-C-T

46462424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544481-G-A

46462424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544481-G-T

46462448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544456-G-T

46462533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544388-G-T

46462715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544220-G-A

46462715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544220-G-T

http://identifiers.org/hco/18/GRCh38#46462751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#77544185-C-A

46462751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544185-C-T

46462807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544144-G-A

46462807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31696
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 77544144-G-T