43729873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24122868-G-A

43729873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24122868-G-T

43729989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24122769-T-C

43731189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24122161-T-C

43731194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24122157-A-G

http://identifiers.org/hco/19/GRCh38#43731217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24122134-C-A

43731217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24122134-C-T

http://identifiers.org/hco/19/GRCh38#43731226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24122125-C-A

http://identifiers.org/hco/19/GRCh38#43731374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24122018-C-A

43731374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24122018-C-T

http://identifiers.org/hco/19/GRCh38#43731448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24121947-A-C

43731448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24121947-A-T

43731536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24121867-C-G

43731536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24121867-C-T

43731563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24121833-G-A

43731787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24121658-G-C

43731787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24121658-G-T

http://identifiers.org/hco/19/GRCh38#43731809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24121631-C-A

43731868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24121597-C-G

43731868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24121597-C-T

43731921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24121554-G-C

43731964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24121533-T-C

43732125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24121406-T-A

43732126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24121405-G-A

43732126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24121405-G-T

http://identifiers.org/hco/19/GRCh38#43732197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24121349-C-A

43732197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24121349-C-T

43732364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24121227-T-A

43732414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24121188-T-G

43732415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24121187-G-A

43732415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24121187-G-T

43732575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24121059-A-T

43732602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24121033-T-A

http://identifiers.org/hco/19/GRCh38#43732792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24120763-A-C

43732797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24120758-C-T

43732912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24120633-A-G

http://identifiers.org/hco/19/GRCh38#43733134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24120476-C-A

43733134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron variant
orthologous variants: 24120476-C-T

43733290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron variant
orthologous variants: 24120404-T-C

43733290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron variant
orthologous variants: 24120404-T-G

43733310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron variant
orthologous variants: 24120378-G-A

43733500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24120193-G-A

43733599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24120121-C-T

43733724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24120008-T-C

43733724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24120008-T-G

http://identifiers.org/hco/19/GRCh38#43734015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24119729-C-A

43734015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24119729-C-G

43734015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24119729-C-T

43734052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24119695-G-C

43734069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24119678-G-A

http://identifiers.org/hco/19/GRCh38#43734075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24119672-C-A

43734075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24119672-C-G

43734075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24119672-C-T

http://identifiers.org/hco/19/GRCh38#43734362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24119570-C-A

http://identifiers.org/hco/19/GRCh38#43734367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24119565-C-A

43734367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24119565-C-T

43734409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24119523-G-A

43734409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24119523-G-T

43734442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24119490-T-C

http://identifiers.org/hco/19/GRCh38#43734549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24119387-C-A

43734556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24119380-G-A

43734556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24119380-G-C

43734556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24119380-G-T

43734564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24119374-G-A

43734564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24119374-G-T

http://identifiers.org/hco/19/GRCh38#43734595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24119343-C-A

43734595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24119343-C-T

43737479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116526-A-G

43737495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116512-G-A

43737495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116512-G-C

43737495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116512-G-T

http://identifiers.org/hco/19/GRCh38#43737496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24116511-A-C

43737496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116511-A-T

43737508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116499-G-A

43737508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116499-G-T

43737536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116486-T-C

http://identifiers.org/hco/19/GRCh38#43737556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24116466-C-A

43737648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24116378-C-T

43737691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116329-G-C

http://identifiers.org/hco/19/GRCh38#43737694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24116326-C-A

43737694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116326-C-T

43737706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116314-G-A

43737740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116298-A-G

http://identifiers.org/hco/19/GRCh38#43737745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24116293-C-A

http://identifiers.org/hco/19/GRCh38#43737752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24116286-C-A

43737752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116286-C-G

43737752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116286-C-T

43737754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116284-G-A

43737756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116282-A-G

43737778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116258-G-T

http://identifiers.org/hco/19/GRCh38#43737786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24116250-C-A

43737786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116250-C-G

43737786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116250-C-T

http://identifiers.org/hco/19/GRCh38#43737791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24116245-A-C

43737791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116245-A-G

43737815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116201-T-C

43737815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116201-T-G

43737816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116200-G-A

43737816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116200-G-C

43737816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24116200-G-T

http://identifiers.org/hco/19/GRCh38#43737838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24116176-C-A

43737868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24116146-T-C

http://identifiers.org/hco/19/GRCh38#43737957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24116092-C-A

http://identifiers.org/hco/19/GRCh38#43738040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24116054-C-A

43738044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24116053-C-T

43738232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24115895-A-G

43738243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24115884-T-C

http://identifiers.org/hco/19/GRCh38#43738322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24115835-C-A

http://identifiers.org/hco/19/GRCh38#43738335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24115822-A-C

43738338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24115819-A-G

43738341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24115807-A-G

43738476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24115700-A-G

43738732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24115477-T-C

43738878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24115391-C-T

http://identifiers.org/hco/19/GRCh38#43738900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24115369-C-A

43739073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24115268-G-A

43739111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24115238-A-G

43739350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114998-G-A

43739556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114818-G-A

43739600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114790-G-A

43739612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114778-A-G

43739645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114755-A-G

43739645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114755-A-T

http://identifiers.org/hco/19/GRCh38#43739673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24114728-C-A

43739757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114649-T-C

43739819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114603-G-A

43739819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114603-G-C

http://identifiers.org/hco/19/GRCh38#43739845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24114576-C-A

43739845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114576-C-T

http://identifiers.org/hco/19/GRCh38#43739855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24114566-C-A

43739855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24114566-C-T

43739871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114555-T-G

http://identifiers.org/hco/19/GRCh38#43739875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24114551-C-A

43739875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114551-C-T

http://identifiers.org/hco/19/GRCh38#43740011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#24114504-C-A

43740011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24114504-C-T

43740056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24114490-G-C

43740056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24114490-G-T

43740094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 24114486-G-T

43740108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 24114472-T-C

43740291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114293-T-C

43740332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114254-T-A

43740332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114254-T-C

http://identifiers.org/hco/19/GRCh38#43740351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24114226-C-A

43740362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114215-G-A

43740362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24114215-G-T

http://identifiers.org/hco/19/GRCh38#43744716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24107127-C-A

43744716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24107127-C-T

43744730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24107113-G-T

43744731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24107112-G-A

43744731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24107112-G-T

43744733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24107110-G-A

43744733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24107110-G-T

http://identifiers.org/hco/19/GRCh38#43745019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24106850-C-A

43745019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24106850-C-G

43745019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24106850-C-T

43745084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24106793-C-T

43746419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24106259-T-A

43747449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24105548-G-A

43747797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24105211-C-G

43747797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24105211-C-T

43747857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24105151-G-A

43747918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24105091-C-G

43748066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24104936-G-A

43750384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24103158-T-C

43750384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24103158-T-G

43750401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24103141-T-G

43750468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24103072-A-G

43750472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24103068-A-G

http://identifiers.org/hco/19/GRCh38#43750524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24103020-C-A

43750524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24103020-C-T

43750541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24103006-G-A

43750541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24103006-G-T

43750650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24102912-A-T

43750671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24102891-C-T

43750692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24102870-C-T

43750846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24102738-A-G

43750846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24102738-A-T

43751755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24102118-C-T

http://identifiers.org/hco/19/GRCh38#43751801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24102072-C-A

43752096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24101842-T-C

43752169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24101794-G-A

43752169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24101794-G-C

43752234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24101763-T-C

43752307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24101693-T-C

43752315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24101685-T-C

43754578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24099408-G-A

43754578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24099408-G-T

43754611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24099377-G-A

43754611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24099377-G-C

43754611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24099377-G-T

http://identifiers.org/hco/19/GRCh38#43754623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24099355-C-A

http://identifiers.org/hco/19/GRCh38#43754638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24099340-C-A

43754638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24099340-C-G

43754639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24099339-T-C

43754683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099285-C-G

43754683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099285-C-T

http://identifiers.org/hco/19/GRCh38#43754692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24099276-C-A

43754692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099276-C-T

43754703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099266-G-A

43754703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099266-G-T

43754711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099258-T-A

43754711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099258-T-C

43754784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099175-G-A

43754882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099093-A-G

43754897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099076-T-C

http://identifiers.org/hco/19/GRCh38#43754901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#24099072-A-C

43754902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099071-T-G

43754919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25763
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24099062-C-T