31391704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5 prime UTR variant
orthologous variants: 79481981-G-A

31391704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5 prime UTR variant
orthologous variants: 79481981-G-T

31391712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5 prime UTR variant
orthologous variants: 79481988-T-A

31391712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5 prime UTR variant
orthologous variants: 79481988-T-G

31391823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5 prime UTR variant
orthologous variants: 79482074-G-A

31391823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5 prime UTR variant
orthologous variants: 79482074-G-C

31391823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5 prime UTR variant
orthologous variants: 79482074-G-T

31392036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79482284-G-A

31392036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79482284-G-C

31392036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79482284-G-T

http://identifiers.org/hco/17/GRCh38#31392218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79482330-C-A

31392218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79482330-C-T

31392226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79482338-G-A

31392238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79482350-G-A

31392238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79482350-G-C

31392238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79482350-G-T

31392295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79482392-G-A

31392295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79482392-G-T

31392305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79482401-T-A

31392305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79482401-T-C

31392410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79482501-G-T

http://identifiers.org/hco/17/GRCh38#31392746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79482827-C-A

31392746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79482827-C-T

31393253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79483210-G-A

31394121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79483927-A-G

31394654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, undefined
orthologous variants: 79484440-C-T

31394796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79484552-A-T

http://identifiers.org/hco/17/GRCh38#31394953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79484597-C-A

31394953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79484597-C-T

31395185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79484788-A-G

31401381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79487590-G-T

31401383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79487592-G-T

31401610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79487785-G-A

31401772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79487962-T-C

31402078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79488257-C-T

31402405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79489145-A-G

31402818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79489614-G-A

31402818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79489614-G-C

31402894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79489701-G-A

31402894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79489701-G-T

31402897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79489704-T-A

31402897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79489704-T-C

31402915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79489722-G-A

31402915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79489722-G-T

31408483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79494110-C-T

31408943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79494539-T-A

31409094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79494706-G-A

31409134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79494747-G-A

31410661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79495945-G-C

31410832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79496105-C-T

31410889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79496165-A-G

31410954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79496222-G-C

31411735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79496565-T-C

31411754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79496584-G-A

31412082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79496776-A-T

31412191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79496884-G-A

http://identifiers.org/hco/17/GRCh38#31412255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79496940-C-A

31412268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79496953-A-G

http://identifiers.org/hco/17/GRCh38#31412281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79496972-C-A

31413591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79501543-A-G

31413617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79501567-A-G

31413708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79501659-G-T

31413783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79501726-G-A

31413783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79501726-G-T

31413944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79501872-C-T

31413988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79501915-G-A

31414185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79502093-C-T

31414390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79502272-A-G

31414460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79502324-C-T

31414797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79502637-C-T

31415312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79503370-G-A

31415390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79503410-A-T

31415682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79503615-C-T

31415931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79503750-C-G

31415937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79503756-C-T

31416006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79503808-T-C

31424913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79506203-G-A

31424913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79506203-G-T

31425077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79506312-C-G

31425077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79506312-C-T

http://identifiers.org/hco/17/GRCh38#31425235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79506462-A-C

31425235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79506462-A-G

31425246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79506472-C-T

http://identifiers.org/hco/17/GRCh38#31425305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#79506528-C-A

31425309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79506532-C-T

31425404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79506575-A-G

31425501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79506667-T-C

http://identifiers.org/hco/17/GRCh38#31425758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79506901-C-A

31425773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79506916-G-A

31425779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79506921-G-A

http://identifiers.org/hco/17/GRCh38#31425831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79506975-C-A

31426158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79507248-G-A

31426158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79507248-G-T

31426478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79507469-A-G

31426497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79507492-T-A

31427350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79507914-G-A

31427751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79508305-G-A

31427875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79508418-G-A

31427980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79508631-C-T

31428213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79508873-C-T

31428229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79508887-C-T

31428355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79509023-T-C

31428578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79509397-C-T

31428579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79509398-G-A

31428590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79509417-T-A

31428590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79509417-T-C

http://identifiers.org/hco/17/GRCh38#31431732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79510378-C-A

31431732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79510378-C-T

http://identifiers.org/hco/17/GRCh38#31431762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79510406-C-A

31431766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79510410-G-A

31431766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79510410-G-T

http://identifiers.org/hco/17/GRCh38#31431920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79510562-C-A

31431920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79510562-C-T

31432110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79510680-G-T

31433906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511170-T-C

31433931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511194-A-G

http://identifiers.org/hco/17/GRCh38#31433983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79511244-C-A

31433983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511244-C-T

31434056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79511315-T-A

31434056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79511315-T-C

31434128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511390-G-T

http://identifiers.org/hco/17/GRCh38#31434151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79511408-C-A

31434151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511408-C-T

31434159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511412-T-C

http://identifiers.org/hco/17/GRCh38#31434167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79511420-C-A

31434167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511420-C-T

http://identifiers.org/hco/17/GRCh38#31434189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79511443-C-A

http://identifiers.org/hco/17/GRCh38#31434190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79511444-C-A

31434190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511444-C-T

http://identifiers.org/hco/17/GRCh38#31434246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79511496-C-A

31434246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79511496-C-T

31436098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515003-C-T

31436099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515004-G-A

31436283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515169-C-T

31436390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515236-C-T

31436502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515342-A-G

31436555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515393-A-G

31437417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515867-C-T

31437476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79515926-A-G

http://identifiers.org/hco/17/GRCh38#31437493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79515944-A-C

31437542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516000-A-T

31437823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516221-A-G

31438147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516483-T-A

31438212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516543-T-C

31438292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516620-G-A

31438518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516853-C-G

31438532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516867-G-C

31438578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516905-C-T

31438626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516956-C-G

31438626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79516956-C-T

31444329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79520457-A-G

31444494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79520592-A-G

31444604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79520722-G-A

31444716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79520830-C-G

31452598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79525733-C-G

31452618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79525753-T-A

http://identifiers.org/hco/17/GRCh38#31452629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79525764-A-C

31452655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79525780-C-T

31452739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79525853-G-A

31452771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79525885-C-T

31453031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79526094-G-A

31453949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79527067-G-A

http://identifiers.org/hco/17/GRCh38#31454003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79527107-A-C

31454206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79527244-A-T

http://identifiers.org/hco/17/GRCh38#31454254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79527286-A-C

31456561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79529342-T-C

http://identifiers.org/hco/17/GRCh38#31456565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79529346-A-C

31456699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79529439-A-G

31458067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79531069-G-A

31458681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79531690-T-C

31458682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79531691-C-G

31458738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79531745-G-A

31458738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79531745-G-T

31458747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79531754-T-A

31458861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79531856-T-C

31459256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79532169-A-G

31459618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79532483-C-T

http://identifiers.org/hco/17/GRCh38#31459758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79532614-A-C

31459834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79532670-A-T

31459976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79532780-G-C

http://identifiers.org/hco/17/GRCh38#31460069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79532873-A-C

31460467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79533336-T-C

31460640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79533491-C-G

31460720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79533582-T-C

31460723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79533585-A-G

31462594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79534889-G-A

31462594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79534889-G-C

31462931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79535091-C-T

31463054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79535199-C-T

31463133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79535267-A-G

http://identifiers.org/hco/17/GRCh38#31463134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79535268-C-A

31463180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79535302-G-T

31463474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79535518-C-T

31463475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79535519-A-G

31464186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79535624-G-A

31464443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79535873-T-C

31467556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79537731-G-C

31467556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79537731-G-T

31467773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79537860-C-T

http://identifiers.org/hco/17/GRCh38#31468274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#79538308-A-C

31468291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, undefined
orthologous variants: 79538324-G-A

31468295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, undefined
orthologous variants: 79538328-C-T

31468296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, undefined
orthologous variants: 79538329-A-G

31468414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79538425-G-C

31468414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79538425-G-T

31470277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79538747-G-A

31470466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79538944-G-A

31470494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79538972-A-G

31470753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79539190-T-G

31470770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79539206-A-G

31471796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79539295-G-T

31471842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79539373-G-A

31477002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79541564-G-C

31477047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79541625-G-A

http://identifiers.org/hco/17/GRCh38#31477166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79541761-A-C

31479348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79542686-G-A

31479402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79542741-G-A

31479737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79542998-G-A

http://identifiers.org/hco/17/GRCh38#31479767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79543027-C-A

31480073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79543275-C-T

31480089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79543282-C-T

31480204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79543361-C-T

31481011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79543876-C-T

31481128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79543921-A-G

31481146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79543939-C-T

31481421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79544184-A-T

31481559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79544281-C-T

31481889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79544784-C-G

31481889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79544784-C-T

31482113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79544962-T-A

31483247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79545422-G-A

31483266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79545439-C-T

31483279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79545452-C-T

31483357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79545532-C-T

31483366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79545541-A-G

31483405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79545577-G-A

31483454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79545616-T-C

31484439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79547280-A-G

31484703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79548035-C-G

31485140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79549173-T-A

31485244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79549268-T-A

31485399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79549530-A-G

31485474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79549624-T-G

31485631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79549781-G-C

31485733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79549847-T-C

http://identifiers.org/hco/17/GRCh38#31487971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79551374-C-A

31487971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79551374-C-T

http://identifiers.org/hco/17/GRCh38#31487997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79551390-C-A

31487997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79551390-C-T

31488008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79551401-G-A

31488008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79551401-G-C

31488008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79551401-G-T

31488223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79551633-T-C

http://identifiers.org/hco/17/GRCh38#31488257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79551667-A-C

31488257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79551667-A-G

31488257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79551667-A-T

31488385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79551775-G-A

31488385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79551775-G-T

http://identifiers.org/hco/17/GRCh38#31488391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79551781-C-A

31488391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79551781-C-T

31488431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 79551860-A-G

31488432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 79551861-G-A

31488432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 79551861-G-T

31488569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79551964-T-G

31488668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79552033-G-A

31488668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79552033-G-C

31488835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79552221-G-A

http://identifiers.org/hco/17/GRCh38#31488942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79552301-C-A

31489886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79553121-A-G

31490259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79553437-G-A

31490269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79553453-T-C

31490990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79553868-C-T

31491053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79553923-T-C

31491217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79554071-A-G

31491264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79554108-A-T

31491368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79554201-C-T

31491415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79554247-T-C

31491464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79554294-A-G

http://identifiers.org/hco/17/GRCh38#31491497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79554329-A-C

31491530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79554347-C-T

31492052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79554796-C-G

http://identifiers.org/hco/17/GRCh38#31492710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79555331-A-C

31492793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79555391-A-G

31492796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79555394-T-C

31492876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79555444-A-G

31492954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79555520-A-T

31493219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79555753-T-G

http://identifiers.org/hco/17/GRCh38#31493429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79556425-A-C

31493429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79556425-A-G

31493533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79556538-C-G

31493533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79556538-C-T

http://identifiers.org/hco/17/GRCh38#31493619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79556628-C-A

31493619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79556628-C-T

31493713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79556736-C-T

31494998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79557247-T-G

31495094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79557357-T-C

31495177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79557437-T-C

31495199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79557459-G-A

31495213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79557473-C-T

31495957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79557944-T-A

31496189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79558189-G-C

http://identifiers.org/hco/17/GRCh38#31496192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79558194-C-A

31496192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79558194-C-T

31496325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79558321-G-A

31496347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79558343-T-A

31496478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79558547-T-A

31497853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79559631-C-T

31498160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79559856-A-G

31498560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79560138-C-T

31498670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79560246-G-C

31499110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79560572-T-C

31499499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79560772-G-A

31499505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79560779-G-A

31499544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79560794-A-G

31500470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79561571-C-T

31500560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79561666-T-C

31503155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79562356-C-T

31503569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79562659-C-T

31503597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79562687-A-G

31505311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79563800-C-T

31505337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79563825-T-G

31508432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79564180-C-T

31508444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79564192-G-C

31508607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79564331-G-A

31508658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79564375-C-T

31508821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79564521-G-A

31508938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79564603-G-A

31508963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79564628-C-T

http://identifiers.org/hco/17/GRCh38#31509012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79564653-C-A

31509191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79564714-A-G

31509449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79564847-T-C

31509498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79564877-G-A

31509585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79564945-A-G

31509693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79565031-C-T

31510355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79565531-C-G

31510391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79565557-C-T

31510571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79565739-C-T

http://identifiers.org/hco/17/GRCh38#31510741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79565877-A-C

http://identifiers.org/hco/17/GRCh38#31510743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79565879-C-A

http://identifiers.org/hco/17/GRCh38#31511289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79566232-C-A

31511289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79566232-C-T

31511401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79566337-G-A

31511404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79566340-A-G

31511540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79566711-T-C

31511611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79566783-A-G

31511687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79566880-A-G

31511988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79567233-A-G

31512042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79567279-C-G

31512176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79567385-T-A

31512176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79567385-T-C

31512487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79567671-C-T

31512507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79567693-G-A

31512622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79567806-G-A

31512740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79567913-C-T

31512974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79568197-T-A

31514639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79569624-G-A

31514862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79569827-G-C

31514867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79569832-A-G

31514944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79569904-G-A

31517433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79571455-A-G

31517459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79571480-T-C

31517574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79571545-G-A

31517574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79571545-G-T

31517777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79571734-A-G

31517785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79571742-C-T

31517823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79571780-G-A

31520868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79573883-A-T

http://identifiers.org/hco/17/GRCh38#31521007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79574032-C-A

31521007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79574032-C-T

31521045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79574059-A-G

31521090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79574094-T-C

31521091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79574095-G-A

31521091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79574095-G-T

31521103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79574107-A-G

31521103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79574107-A-T

http://identifiers.org/hco/17/GRCh38#31521111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79574117-C-A

31521111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79574117-C-T

31521122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79574128-G-A

31521122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79574128-G-T

31521187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79574188-C-T

31521193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79574194-G-A

31521193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79574194-G-T

31521208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79574209-T-A

31521247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79574248-G-C

31521307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79574308-T-C

31521367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79574368-C-T

31521726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79574742-T-A

31521727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79574743-G-A

31521727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79574743-G-T

http://identifiers.org/hco/17/GRCh38#31521783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79574894-C-A

31521783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79574894-C-T

31521862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79574967-G-C

31521945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79575079-C-T

31521946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79575080-G-A

31521946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79575080-G-C

http://identifiers.org/hco/17/GRCh38#31521957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79575091-C-A

31521957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79575091-C-T

31522058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79575192-C-T

http://identifiers.org/hco/17/GRCh38#31522123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79575223-A-C

31522123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79575223-A-G

http://identifiers.org/hco/17/GRCh38#31522141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79575237-C-A

http://identifiers.org/hco/17/GRCh38#31522145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79575241-C-A

31522147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79575243-G-A

http://identifiers.org/hco/17/GRCh38#31523679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79576006-A-C

31523748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576074-G-A

31523748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576074-G-C

31523780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576104-G-A

31523850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576168-G-T

31524016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576318-T-C

31524017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576319-G-A

31524017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576319-G-T

http://identifiers.org/hco/17/GRCh38#31524024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79576326-C-A

31524024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576326-C-G

31524024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576326-C-T

31524059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576366-T-C

31524059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576366-T-G

31524298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576641-A-G

31524325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576667-A-G

31524374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576745-G-A

31524374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576745-G-T

31524412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576796-G-A

31524412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576796-G-T

31524417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576801-T-C

http://identifiers.org/hco/17/GRCh38#31524419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79576803-C-A

31524419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576803-C-T

http://identifiers.org/hco/17/GRCh38#31524653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79576978-C-A

31524653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576978-C-G

31524662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576987-G-A

31524662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79576987-G-T

31524766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577059-G-C

http://identifiers.org/hco/17/GRCh38#31524774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577063-A-C

31524774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577063-A-G

31524774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577063-A-T

31524798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577083-G-A

31524849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577128-T-C

31524850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577129-G-C

31524850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577129-G-T

http://identifiers.org/hco/17/GRCh38#31524857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577135-C-A

31524861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577139-A-G

http://identifiers.org/hco/17/GRCh38#31524867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577149-C-A

31524867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577149-C-T

31524885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577172-G-A

31524885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577172-G-T

31524889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577176-G-A

31524889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577176-G-T

http://identifiers.org/hco/17/GRCh38#31524897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577184-A-C

31524897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577184-A-G

31524954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577245-A-G

31524979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577275-G-A

31525001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577302-G-T

http://identifiers.org/hco/17/GRCh38#31525010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577314-C-A

31525010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577314-C-T

31525036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577328-G-A

31525036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577328-G-C

31525036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577328-G-T

31525057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577345-G-A

31525057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577345-G-T

http://identifiers.org/hco/17/GRCh38#31525062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577350-A-C

31525062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577350-A-G

31525062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577350-A-T

31525064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577354-G-T

31525069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577359-T-C

http://identifiers.org/hco/17/GRCh38#31525268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577557-C-A

31525268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577557-C-T

31525289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79577578-G-A

31525289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79577578-G-T

31525300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577586-G-A

31525300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577586-G-T

31525304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577590-T-C

31525378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79577641-T-A

31525378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79577641-T-C

http://identifiers.org/hco/17/GRCh38#31525466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577728-C-A

31525466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79577728-C-G

http://identifiers.org/hco/17/GRCh38#31525544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577793-C-A

http://identifiers.org/hco/17/GRCh38#31525634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577854-C-A

31525634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577854-C-T

31525665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577887-G-T

http://identifiers.org/hco/17/GRCh38#31525668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577890-C-A

31525668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577890-C-T

31525687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577906-T-A

31525687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577906-T-C

31525719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577933-G-A

http://identifiers.org/hco/17/GRCh38#31525721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577935-C-A

31525721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577935-C-T

http://identifiers.org/hco/17/GRCh38#31525737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577945-C-A

http://identifiers.org/hco/17/GRCh38#31525745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577953-C-A

31525745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577953-C-G

31525745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577953-C-T

http://identifiers.org/hco/17/GRCh38#31525791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577960-C-A

http://identifiers.org/hco/17/GRCh38#31525800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577968-C-A

31525800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79577968-C-T

http://identifiers.org/hco/17/GRCh38#31525846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79577992-C-A

31525885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578028-A-G

31525885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578028-A-T

http://identifiers.org/hco/17/GRCh38#31525912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79578054-C-A

31525912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578054-C-T

31525933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578096-C-T

http://identifiers.org/hco/17/GRCh38#31526144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79578311-C-A

31526194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578357-T-C

31526212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578373-G-A

31526212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578373-G-T

31526240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578409-G-T

31526276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578449-G-T

31526315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578485-C-T

31526363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578531-C-T

31526375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578541-A-G

http://identifiers.org/hco/17/GRCh38#31526471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79578630-C-A

31526490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578653-G-A

31526490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578653-G-T

31526511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578693-T-C

31526541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578716-G-A

31526541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578716-G-T

http://identifiers.org/hco/17/GRCh38#31526655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79578790-C-A

31526655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578790-C-G

31526655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578790-C-T

31527103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578902-T-C

31527104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578903-G-T

http://identifiers.org/hco/17/GRCh38#31527128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79578926-A-C

31527128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79578926-A-T

http://identifiers.org/hco/17/GRCh38#31527724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79580333-C-A

http://identifiers.org/hco/17/GRCh38#31527745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79580350-C-A

31527745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79580350-C-T

http://identifiers.org/hco/17/GRCh38#31527759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79580360-C-A

31527760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79580361-A-T

31527779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79580373-G-A

31527779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79580373-G-T

http://identifiers.org/hco/17/GRCh38#31527972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79580597-C-A

31528050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79580802-G-A

31528050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79580802-G-T

http://identifiers.org/hco/17/GRCh38#31528082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79580834-C-A

31528086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79580838-G-A

31528086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79580838-G-T

31528299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79581219-G-A

31528299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79581219-G-T

31528378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79581255-C-T

31528399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79581277-G-A

31528537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: synonymous variant
orthologous variants: 79581415-G-A

31528603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79581480-G-A

31528609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79581486-C-G

31528609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79581486-C-T

31528676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: synonymous variant
orthologous variants: 79581554-C-T

31528760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: synonymous variant
orthologous variants: 79581635-G-A

31528760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: missense variant
orthologous variants: 79581635-G-C

31528835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79581709-G-A

31528835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79581709-G-C

31528835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79581709-G-T

31528858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79581724-A-G

31529888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79582267-G-A

31529916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79582295-C-T

31530267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79582524-T-C

31530281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79582538-G-A

31530281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79582538-G-C

31530340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: synonymous variant
orthologous variants: 79582596-G-A

31530340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: synonymous variant
orthologous variants: 79582596-G-C

31530343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: synonymous variant
orthologous variants: 79582599-G-A

http://identifiers.org/hco/17/GRCh38#31530397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79582653-A-C

31530397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: synonymous variant
orthologous variants: 79582653-A-T

31530478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79582754-A-G

http://identifiers.org/hco/17/GRCh38#31530531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79582807-C-A

31530531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79582807-C-G

31530531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79582807-C-T

http://identifiers.org/hco/17/GRCh38#31530596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79582899-C-A

31530831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79583018-G-A

31530850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79583036-G-A

31530850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79583036-G-T

http://identifiers.org/hco/17/GRCh38#31530899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79583078-A-C

31530942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79583107-A-G

31530958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron variant
orthologous variants: 79583123-C-T

http://identifiers.org/hco/17/GRCh38#31530976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79583138-C-A

31531085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79583200-T-A

31531085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79583200-T-C

31531085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79583200-T-G

31531092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79583207-G-A

31531092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79583207-G-T

31531157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583244-C-T

31531193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583292-A-G

http://identifiers.org/hco/17/GRCh38#31531194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79583293-C-A

31531223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583312-T-C

31531223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583312-T-G

31531224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583313-G-C

31531224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583313-G-T

http://identifiers.org/hco/17/GRCh38#31531244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79583335-C-A

31531244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583335-C-T

http://identifiers.org/hco/17/GRCh38#31531245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79583336-A-C

31531245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583336-A-G

31531245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583336-A-T

31531251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583342-G-T

31531370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583434-A-G

31531507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79583483-T-G

http://identifiers.org/hco/17/GRCh38#31531587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79583520-C-A

31531751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79583682-G-A

31531751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79583682-G-C

31531821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79583754-C-T

http://identifiers.org/hco/17/GRCh38#31531962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79583876-C-A

31531962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79583876-C-T

31531984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79583898-A-G

31531984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79583898-A-T

31531997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79583910-G-A

31531997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79583910-G-T

31532155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584045-G-T

31532276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584164-G-A

31532276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584164-G-T

http://identifiers.org/hco/17/GRCh38#31532310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79584188-C-A

31532310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584188-C-T

31532453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584317-T-C

31532453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584317-T-G

31532464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584343-A-G

31532465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584344-G-A

31532519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584382-G-A

31532519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584382-G-C

31532543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584401-T-A

31532630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584472-G-A

31532655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584487-A-G

http://identifiers.org/hco/17/GRCh38#31532694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79584508-C-A

31532694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584508-C-G

31532883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584662-T-C

31532886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584665-T-C

http://identifiers.org/hco/17/GRCh38#31532934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79584709-C-A

31532940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584715-A-G

31533045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584830-T-C

31533045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584830-T-G

31533081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79584861-G-A

http://identifiers.org/hco/17/GRCh38#31533216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79584988-C-A

31533330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79585086-T-A

31533330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79585086-T-C

31533360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79585111-G-T

31533367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79585114-C-T

31533455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79585170-G-A

31533455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79585170-G-T

http://identifiers.org/hco/17/GRCh38#31533528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79585236-C-A

31533573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79585256-G-T

31533584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79585267-A-G

31533869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79585548-A-G

http://identifiers.org/hco/17/GRCh38#31533949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79585622-C-A

31534071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79585758-G-A

31534143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79585815-T-C

31534143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79585815-T-G

http://identifiers.org/hco/17/GRCh38#31536562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79587299-C-A

http://identifiers.org/hco/17/GRCh38#31536577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79587312-C-A

31536577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587312-C-G

http://identifiers.org/hco/17/GRCh38#31536704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79587414-C-A

31536704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587414-C-T

31536737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587445-A-G

31536794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587490-C-T

31536799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587495-A-G

31536888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587628-C-T

http://identifiers.org/hco/17/GRCh38#31536901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79587641-C-A

31536901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587641-C-T

31536914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587647-A-G

31536947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587680-C-T

http://identifiers.org/hco/17/GRCh38#31536998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79587737-A-C

31536998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587737-A-G

31536998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587737-A-T

31537122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587846-G-A

31537122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587846-G-T

31537133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587851-T-A

31537133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587851-T-C

http://identifiers.org/hco/17/GRCh38#31537223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79587934-C-A

31537223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587934-C-T

31537225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587935-G-A

31537225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587935-G-T

31537283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587990-G-A

31537283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587990-G-C

31537283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79587990-G-T

31537307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588010-G-T

31537474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588164-G-C

31537474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588164-G-T

31537551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588242-C-T

http://identifiers.org/hco/17/GRCh38#31537724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79588399-C-A

31537724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588399-C-T

31537751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588426-C-T

31537839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588517-A-G

31537841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588519-A-G

31537848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588523-G-A

31537848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588523-G-T

31537895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588569-C-T

31537897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588571-A-G

31537897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588571-A-T

31538037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: 79588686-G-A

http://identifiers.org/hco/17/GRCh38#31538182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30267
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#79588814-C-A