http://identifiers.org/hco/1/GRCh38#201190837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#135912017-C-A

http://identifiers.org/hco/1/GRCh38#201190860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#135911984-C-A

201190860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 135911984-C-G

201190860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 135911984-C-T

201190928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911929-G-A

201190928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911929-G-T

201190962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911896-G-A

201191029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911829-G-T

201191097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911764-A-G

201191352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911555-T-C

201191468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911444-G-A

201191524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911403-G-A

201191556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911371-G-A

201191570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911358-T-C

201191881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135911100-G-A

201192090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910940-G-A

201192101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910920-T-C

201192339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910707-T-C

201192362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910680-G-A

201192370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910672-G-A

201192920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910462-T-G

201193115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910288-T-A

201193179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910218-G-A

201193184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910213-T-G

http://identifiers.org/hco/1/GRCh38#201193210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135910187-C-A

201193210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910187-C-T

201193230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910168-T-C

http://identifiers.org/hco/1/GRCh38#201193237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135910161-C-A

201193237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910161-C-T

201193315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910091-A-G

http://identifiers.org/hco/1/GRCh38#201193341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135910067-C-A

201193341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910067-C-G

201193341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910067-C-T

http://identifiers.org/hco/1/GRCh38#201193349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135910059-A-C

201193349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910059-A-G

201193349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135910059-A-T

201193756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909996-T-A

201193757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909995-T-C

201193897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909882-G-C

201193996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909803-C-T

http://identifiers.org/hco/1/GRCh38#201194003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135909796-A-C

201194003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909796-A-G

201194006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909793-A-G

201194016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909779-A-G

http://identifiers.org/hco/1/GRCh38#201194041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135909748-C-A

201194041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909748-C-G

201194041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909748-C-T

201194064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909737-G-T

http://identifiers.org/hco/1/GRCh38#201194177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135909664-C-A

201194177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135909664-C-T

201194304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909537-G-A

http://identifiers.org/hco/1/GRCh38#201194347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135909491-C-A

201194375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909459-A-G

http://identifiers.org/hco/1/GRCh38#201194403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135909436-C-A

201194403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909436-C-G

201194403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909436-C-T

201194475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135909363-G-A

201195067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135908229-C-T

http://identifiers.org/hco/1/GRCh38#201195311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135908100-C-A

201195427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135908097-C-T

201195496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135908045-T-C

201195670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907894-C-T

201195726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907840-G-A

201195726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907840-G-T

201195758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907807-A-G

201195770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907795-A-T

http://identifiers.org/hco/1/GRCh38#201195796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135907769-C-A

201195796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907769-C-T

201195799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907766-C-T

201195831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 135907748-T-C

201195844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135907735-A-T

201195940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135907639-A-T

201196013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907568-A-G

201196117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907473-T-G

201196281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907339-T-C

201196330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907291-T-C

201196330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135907291-T-G

201196847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906430-T-C

http://identifiers.org/hco/1/GRCh38#201196980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135906292-A-C

201196980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906292-A-G

201196981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906291-A-G

201196981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906291-A-T

201196992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906280-T-C

201197004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906269-T-A

201197125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906159-T-C

201197126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906158-A-T

201197149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906135-T-A

201197149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906135-T-C

201197149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906135-T-G

http://identifiers.org/hco/1/GRCh38#201197152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135906132-C-A

201197171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906113-G-T

http://identifiers.org/hco/1/GRCh38#201197197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135906084-C-A

201197203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906078-T-C

201197203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135906078-T-G

201197266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135906015-G-T

201197287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135905994-G-A

201197305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135905976-A-T

http://identifiers.org/hco/1/GRCh38#201197365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135905921-C-A

201197365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905921-C-T

http://identifiers.org/hco/1/GRCh38#201197405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135905896-A-C

201197405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905896-A-G

201197405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905896-A-T

http://identifiers.org/hco/1/GRCh38#201197410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135905891-A-C

201197410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905891-A-G

201197410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905891-A-T

201197430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905879-G-A

201197431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905878-G-A

201197431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905878-G-C

201197431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905878-G-T

http://identifiers.org/hco/1/GRCh38#201197447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135905863-C-A

201197447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905863-C-T

201197464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905846-G-A

201197489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905821-C-T

201197490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905820-A-G

201197611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905709-A-G

201197760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905569-A-G

http://identifiers.org/hco/1/GRCh38#201197901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135905431-A-C

http://identifiers.org/hco/1/GRCh38#201197902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135905430-C-A

201197902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905430-C-T

201197903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905429-G-A

201197903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905429-G-C

201197925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905405-G-A

201197935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905395-G-A

201197935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905395-G-T

201198795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905158-T-A

201198868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905093-G-A

201198939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135905027-T-C

201199086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904915-C-G

201199086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904915-C-T

201199211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904819-G-A

201199295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904737-T-C

http://identifiers.org/hco/1/GRCh38#201199296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135904736-C-A

201199296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904736-C-T

201199386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 135904646-G-A

201199387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904645-A-G

201199396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904636-A-T

201199443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904607-T-C

http://identifiers.org/hco/1/GRCh38#201199470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135904575-C-A

201199470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904575-C-T

http://identifiers.org/hco/1/GRCh38#201199485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135904560-C-A

201199515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904537-G-T

http://identifiers.org/hco/1/GRCh38#201199555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135904503-C-A

201199651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135904410-A-G

201199700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904363-A-G

201199704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904359-A-G

http://identifiers.org/hco/1/GRCh38#201199743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135904320-C-A

201199743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904320-C-T

201199792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904271-G-C

201199792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904271-G-T

201199960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904092-G-A

201199971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135904081-T-G

201200152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135903889-A-G

201200180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135903861-G-T

201200337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135903699-G-A

201200337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135903699-G-T

201200343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135903693-G-A

201200343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135903693-G-T

http://identifiers.org/hco/1/GRCh38#201200382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135903654-A-C

http://identifiers.org/hco/1/GRCh38#201200514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135903545-C-A

201200522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135903537-G-A

201200522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135903537-G-T

201200852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135903235-G-A

201200852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135903235-G-T

http://identifiers.org/hco/1/GRCh38#201200866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135903220-C-A

201200866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135903220-C-T

201201429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902798-G-A

201201568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902696-G-C

201201568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902696-G-T

201201625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902639-G-A

201201625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902639-G-T

http://identifiers.org/hco/1/GRCh38#201201642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135902622-A-C

201201642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902622-A-T

201201860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902459-G-A

201201860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902459-G-C

201201860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902459-G-T

201201871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902448-G-A

201201871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902448-G-C

201201871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902448-G-T

201202304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902206-C-T

http://identifiers.org/hco/1/GRCh38#201202335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135902191-C-A

201202335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902191-C-T

201202436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902090-C-T

201202527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135902003-G-C

201203527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135901445-A-G

201203632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135901334-G-A

201203632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135901334-G-T

http://identifiers.org/hco/1/GRCh38#201203634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135901332-C-A

201203730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 135901258-G-A

201203730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 135901258-G-T

201203750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135901238-A-G

201203750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135901238-A-T

201203858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 135901130-G-A

201203931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135901057-T-G

201203937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135901051-T-C

201203942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135901046-A-G

201203942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135901046-A-T

201203985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135901018-T-A

201204034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135900970-G-A

201204034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135900970-G-C

201204034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135900970-G-T

201204250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135900809-G-A

201204670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135900442-T-C

201204864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135900162-C-T

201204885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135900151-T-C

http://identifiers.org/hco/1/GRCh38#201204922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135900104-A-C

201204974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135900024-G-T

201205068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135899928-T-A

201205068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 135899928-T-C

201205131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135899865-G-A

http://identifiers.org/hco/1/GRCh38#201205189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135899807-C-A

201205189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135899807-C-T

http://identifiers.org/hco/1/GRCh38#201205209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135899787-C-A

201205209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135899787-C-T

201205306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135899690-T-A

201205355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 135899641-G-A

201205466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135899516-A-G

http://identifiers.org/hco/1/GRCh38#201205484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135899497-C-A

201205484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135899497-C-T

201205502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135899479-A-G

201205610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135899377-G-A

201205611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135899376-G-T

201205637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135899350-C-T

http://identifiers.org/hco/1/GRCh38#201206152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#135898827-C-A

201206204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135898775-G-A

201206204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135898775-G-T

201206313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135898687-G-A

201206313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135898687-G-C

http://identifiers.org/hco/1/GRCh38#201206378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135898622-A-C

201206403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135898597-A-G

201206413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135898587-A-G

201206500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898500-C-G

201206507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135898493-A-G

201206507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898493-A-T

201206509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898491-A-G

201206538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898462-A-G

201206538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898462-A-T

201206539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898461-G-A

201206586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898414-C-T

201206591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135898409-T-G

201206595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898405-G-T

http://identifiers.org/hco/1/GRCh38#201206596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135898404-C-A

201206634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898366-A-G

201206677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898323-A-T

http://identifiers.org/hco/1/GRCh38#201206678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135898322-A-C

201206678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135898322-A-G

201206680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898320-T-C

http://identifiers.org/hco/1/GRCh38#201206694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135898306-C-A

http://identifiers.org/hco/1/GRCh38#201206720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135898280-C-A

201206720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898280-C-G

201206720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135898280-C-T

201206731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898269-G-A

201206731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898269-G-C

201206731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898269-G-T

201206733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135898267-C-T

201206735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135898265-G-A

201206771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135898229-G-A

201206771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898229-G-C

201206771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898229-G-T

http://identifiers.org/hco/1/GRCh38#201206805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135898198-A-C

201206836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898167-G-A

201206836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898167-G-C

201206853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898153-G-A

201206853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898153-G-C

201206857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135898149-G-A

201206857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898149-G-C

201206857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898149-G-T

201206875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898131-T-A

201206878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898128-G-A

201206878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898128-G-T

201206894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898112-C-G

201206894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135898112-C-T

201206901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898105-G-A

201206901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898105-G-T

201206908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898098-G-T

201206916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898090-A-G

201206959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135898047-G-A

201207021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897994-G-A

201207031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897984-G-A

201207032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897983-G-A

201207059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897956-T-C

201207069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897946-G-A

201207156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897862-G-A

201207156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135897862-G-T

http://identifiers.org/hco/1/GRCh38#201207161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135897857-A-C

201207190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897843-T-C

201207199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897834-G-A

201207234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897799-C-T

201207311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897722-A-T

201207364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897669-G-A

201207412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897621-G-C

http://identifiers.org/hco/1/GRCh38#201207454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135897579-A-C

201207454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897579-A-G

201207470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897563-G-A

http://identifiers.org/hco/1/GRCh38#201207476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135897557-C-A

201207482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897551-A-T

201207487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897546-A-G

201207492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897541-G-T

201207502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897531-G-A

201207651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135897382-G-T

201207675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897358-G-A

201207675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897358-G-T

201207728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897317-G-A

201207728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897317-G-C

201207823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897222-C-T

201207828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897217-G-A

201207844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897201-G-T

201207850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897195-G-A

201207871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897174-T-G

201207883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897162-C-T

201207887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897158-T-C

201207938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897107-G-A

201207938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897107-G-C

201207938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897107-G-T

201207966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897079-G-T

201207990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135897052-T-C

201208004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135897038-C-T

201208093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896946-C-T

201208138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896901-T-G

201208181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896858-A-G

201208193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896846-T-C

201208250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896789-T-A

201208250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896789-T-C

201208250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896789-T-G

201208329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896719-G-A

201208329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896719-G-T

201208361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896687-G-A

201208361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896687-G-T

201208485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896566-G-A

http://identifiers.org/hco/1/GRCh38#201208546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#135896505-C-A

201208546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135896505-C-G

201208640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896411-G-C

201208662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896389-G-A

201208662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896389-G-C

201208663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896388-G-A

201208663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896388-G-T

201208728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896323-G-A

201208728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135896323-G-T

201208739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896312-A-T

201208748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896303-G-A

201208754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896297-T-C

201208781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896270-G-A

201208781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896270-G-T

201208784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896267-T-A

201208818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896233-G-A

201208836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896215-G-A

201208842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896209-G-A

201208865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135896186-T-G

201208866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896185-A-G

201209006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896054-G-A

201209006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896054-G-T

201209027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896033-T-C

201209030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896030-G-A

201209030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896030-G-T

201209040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896020-G-A

201209058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896002-G-C

201209061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895985-G-A

201209061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895985-G-T

201209111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895937-T-A

201209111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895937-T-C

201209111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895937-T-G

201209157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895903-T-G

201209177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895882-G-A

201209177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895882-G-T

201209190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896323-G-A

201209191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896322-G-A

201209191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896322-G-C

201209201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896312-A-T

201209204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896309-G-A

201209210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896303-G-A

201209216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896297-T-A

201209243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896270-A-G

201209243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896270-A-T

201209246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896267-A-G

201209246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896267-A-T

201209279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896233-A-G

201209298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896215-A-G

201209378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135896186-T-A

201209378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896186-T-C

http://identifiers.org/hco/1/GRCh38#201209425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135896139-C-A

201209425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896139-C-T

201209616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896323-G-A

201209630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896309-G-A

201209630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896309-G-C

201209636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896303-G-T

201209642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896297-T-C

201209669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896270-A-G

201209706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896233-G-A

201209724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896215-G-A

http://identifiers.org/hco/1/GRCh38#201209746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135896139-C-A

201209746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896139-C-T

201209753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896186-T-A

201209753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896186-T-C

201209800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896139-C-T

201209801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896138-A-G

201209801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896138-A-T

http://identifiers.org/hco/1/GRCh38#201209829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895869-A-C

201209829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895869-A-G

201209829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135895869-A-T

http://identifiers.org/hco/1/GRCh38#201209835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895863-A-C

201209835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895863-A-G

201209857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895839-G-A

http://identifiers.org/hco/1/GRCh38#201209866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895830-A-C

201209866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895830-A-G

201209911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895776-G-A

201209911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895776-G-C

201209911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895776-G-T

201209941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895717-G-A

201209941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895717-G-C

201209941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895717-G-T

201210041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895553-T-C

http://identifiers.org/hco/1/GRCh38#201210181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895410-A-C

201210181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895410-A-G

201210181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895410-A-T

201210203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895378-T-G

201210216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895365-G-A

201210216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895365-G-C

201210216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895365-G-T

201210264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895336-G-A

201210264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135895336-G-T

201210301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895299-G-C

201210434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896054-G-A

201210455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135896033-T-A

201210455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896033-T-C

201210458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896030-G-A

201210461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896027-G-A

201210461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896027-G-T

201210468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896020-G-A

201210468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896020-G-C

201210468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896020-G-T

201210588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896323-G-A

201210588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896323-G-C

201210588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135896323-G-T

201210589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896322-G-A

201210589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896322-G-C

201210589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896322-G-T

http://identifiers.org/hco/1/GRCh38#201210602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135896309-A-C

201210602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896309-A-G

201210602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896309-A-T

201210608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896303-G-A

201210614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896297-T-G

201210641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896270-A-G

http://identifiers.org/hco/1/GRCh38#201210644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135896267-A-C

201210678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896233-G-A

201210696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896215-G-A

201210725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896186-C-G

201210725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896186-C-T

201210726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896185-A-G

201210726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896185-A-T

http://identifiers.org/hco/1/GRCh38#201210772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135896139-C-A

201210773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896138-A-T

201210840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896233-G-A

201210858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896215-G-A

201210858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896215-G-C

201210864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896209-G-A

201210864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896209-G-C

201210864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896209-G-T

201210887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896186-T-C

201210888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896185-A-G

201210888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896185-A-T

http://identifiers.org/hco/1/GRCh38#201210934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135896139-C-A

201210934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896139-C-G

201210975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895903-T-C

http://identifiers.org/hco/1/GRCh38#201211000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895882-A-C

201211000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895882-A-G

http://identifiers.org/hco/1/GRCh38#201211012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895874-C-A

201211012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895874-C-G

201211012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895874-C-T

201211017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895869-G-A

201211017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895869-G-C

201211017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135895869-G-T

http://identifiers.org/hco/1/GRCh38#201211023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895863-A-C

201211023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895863-A-G

http://identifiers.org/hco/1/GRCh38#201211054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895830-A-C

201211054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895830-A-G

201211218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895564-G-A

201211218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895564-G-T

201211229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895553-T-C

201211301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895478-A-G

http://identifiers.org/hco/1/GRCh38#201211355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895424-A-C

201211365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895414-G-A

201211365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895414-G-T

201211369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895410-G-A

201211369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895410-G-C

201211391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895378-T-G

201211404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895365-G-A

201211410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895350-A-G

201211419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895340-G-A

201211419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895340-G-T

201211423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895336-G-A

201211423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895336-G-C

201211423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895336-G-T

201211453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895310-G-A

201211453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895310-G-T

201211466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895299-G-A

201211466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895299-G-C

201211466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895299-G-T

201211488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: -G-C

201211512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895906-G-A

201211535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895887-T-C

http://identifiers.org/hco/1/GRCh38#201211536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895886-A-C

201211536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895886-A-G

http://identifiers.org/hco/1/GRCh38#201211582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895850-C-A

201211582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895850-C-G

201211582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895850-C-T

201211669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896322-A-G

201211682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896309-C-T

http://identifiers.org/hco/1/GRCh38#201211688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#135896303-C-A

201211688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135896303-C-G

201211688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896303-C-T

http://identifiers.org/hco/1/GRCh38#201211724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135896267-A-C

201211758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896233-G-A

201211776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896215-A-G

201211782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896209-C-G

201211782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896209-C-T

201211805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896186-T-C

201211806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135896185-A-G

201211892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896054-G-A

201211892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896054-G-T

http://identifiers.org/hco/1/GRCh38#201211895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135896051-A-C

201211913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135896033-T-C

201211961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895985-G-C

201212096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895874-C-G

201212101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895869-A-T

201212107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895863-G-A

201212107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895863-G-T

201212131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895839-G-A

201212131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895839-G-T

201212140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895830-A-G

201212149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895821-G-A

201212149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895821-G-T

201212194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895776-G-A

201212194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895776-G-T

http://identifiers.org/hco/1/GRCh38#201212253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895717-C-A

201212253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135895717-C-T

201212286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895684-A-G

http://identifiers.org/hco/1/GRCh38#201212318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895652-C-A

201212318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895652-C-T

201212406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895564-G-T

201212417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895553-T-C

201212492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895478-A-T

201212545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895446-G-A

201212567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895424-A-G

201212577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895414-G-A

201212577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895414-G-C

201212577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895414-G-T

201212581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895410-G-C

201212581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895410-G-T

201212626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895365-G-A

201212626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895365-G-C

201212626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895365-G-T

201212718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895267-G-A

201212719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895266-G-A

201212719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895266-G-T

201212744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895241-T-A

201212747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895238-A-G

201212753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895232-G-A

201212768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135895217-G-A

201212768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895217-G-T

201212791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895196-G-T

201212835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895183-T-C

201212836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895182-C-G

201212856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 135895162-C-T

http://identifiers.org/hco/1/GRCh38#201212925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135895093-C-A

201212925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895093-C-T

201212957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895061-C-T

201212960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895058-A-G

201212969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895049-G-C

201212969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895049-G-T

201212990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135895028-T-C

201212996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135895022-G-T

201213062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135894956-T-A

201213062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 135894956-T-C

201213063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135894955-G-A

201213078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135894940-C-G

201213078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 135894940-C-T

http://identifiers.org/hco/1/GRCh38#201213136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135894897-A-C

http://identifiers.org/hco/1/GRCh38#201213225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135894808-C-A

201213225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 135894808-C-T

201213250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135894783-G-A

201213259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135894774-A-G

201213259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135894774-A-T

201213288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135894745-G-A

201213288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135894745-G-T

201213362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135894671-A-G

201213396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135894627-G-A

http://identifiers.org/hco/1/GRCh38#201213397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135894626-C-A

201213409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135894616-G-A

201213479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135894554-C-T

http://identifiers.org/hco/1/GRCh38#201213495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135894538-C-A

201213495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135894538-C-T

201213518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135894515-C-T

http://identifiers.org/hco/1/GRCh38#201213524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135894509-C-A

201213524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135894509-C-T

201213715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135894324-T-C

201213715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135894324-T-G

201213846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135894183-C-T

201213863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135894166-T-C

201213918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135894108-C-T

201213945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135894072-C-T

http://identifiers.org/hco/1/GRCh38#201214061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135894022-C-A

201214061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135894022-C-T

http://identifiers.org/hco/1/GRCh38#201214069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135894014-C-A

201214069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135894014-C-G

201214069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135894014-C-T

201214198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135893904-A-G

201214209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135893893-G-T

201214240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135893862-C-T

201214296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135893806-G-A

201214312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135893792-C-T

201214337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135893756-G-T

201214817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135893372-T-C

http://identifiers.org/hco/1/GRCh38#201215048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135893134-C-A

201215048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135893134-C-T

201215055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135893127-G-A

http://identifiers.org/hco/1/GRCh38#201215226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135892997-C-A

201215226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892997-C-T

201215239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892984-G-T

201215289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892944-T-C

201215304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892929-A-G

201215431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892798-A-T

http://identifiers.org/hco/1/GRCh38#201215482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135892771-A-C

201215482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892771-A-G

201215591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135892646-G-C

201215614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135892623-T-C

201215771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135892466-C-T

http://identifiers.org/hco/1/GRCh38#201215790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135892447-A-C

201215790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135892447-A-G

http://identifiers.org/hco/1/GRCh38#201215830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135892407-A-C

201215830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135892407-A-G

201215881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135892356-G-A

http://identifiers.org/hco/1/GRCh38#201215901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135892336-C-A

201215901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135892336-C-T

201215909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135892328-G-A

201215909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135892328-G-T

201215910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135892327-G-A

201215950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135892288-T-C

http://identifiers.org/hco/1/GRCh38#201216137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135892114-C-A

201216153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892098-G-C

201216153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892098-G-T

201216171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892073-G-A

201216171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892073-G-T

201216187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892057-G-A

http://identifiers.org/hco/1/GRCh38#201216220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135892027-A-C

201216220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892027-A-G

201216222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135892025-G-T

201216265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891980-T-A

201216351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891864-G-A

201216351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891864-G-T

201216359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891856-G-A

201216359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891856-G-T

201216463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135891784-A-G

201216474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135891773-G-A

201216474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135891773-G-T

201216559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135891688-A-G

201216561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135891686-T-C

201216698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135891549-C-G

201216708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135891539-G-A

201216708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135891539-G-T

201216761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135891486-A-G

201216761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135891486-A-T

201216807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891442-T-C

201216889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891358-G-A

201216889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891358-G-T

201216891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891356-G-A

http://identifiers.org/hco/1/GRCh38#201216893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135891354-C-A

201217136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891117-A-T

201217139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891114-T-C

201217142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891111-G-A

201217142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891111-G-T

http://identifiers.org/hco/1/GRCh38#201217175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135891081-C-A

201217175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891081-C-G

http://identifiers.org/hco/1/GRCh38#201217176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135891080-A-C

201217176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891080-A-G

201217202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891052-G-A

201217202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891052-G-C

201217202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891052-G-T

http://identifiers.org/hco/1/GRCh38#201217211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135891043-C-A

http://identifiers.org/hco/1/GRCh38#201217231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135891021-C-A

201217232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891020-A-G

201217232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891020-A-T

201217240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891012-G-A

201217240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135891012-G-T

201217408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135890857-G-A

201217478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135890783-T-G

201217505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135890741-G-A

201217505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135890741-G-C

201217505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135890741-G-T

http://identifiers.org/hco/1/GRCh38#201217533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135890713-C-A

201217533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135890713-C-G

201217533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135890713-C-T

201217576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135890647-A-T

http://identifiers.org/hco/1/GRCh38#201217578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135890645-C-A

201217578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135890645-C-T

201218384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889997-G-A

201218384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889997-G-T

201218390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889991-A-G

http://identifiers.org/hco/1/GRCh38#201218393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135889988-C-A

201218406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889974-G-T

201218459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889923-G-T

http://identifiers.org/hco/1/GRCh38#201218479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135889904-C-A

201218479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889904-C-T

http://identifiers.org/hco/1/GRCh38#201218480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135889903-C-A

201218502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889881-G-T

201218562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135889819-G-C

201218585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135889796-C-T

http://identifiers.org/hco/1/GRCh38#201218590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135889791-C-A

http://identifiers.org/hco/1/GRCh38#201218596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135889785-C-A

http://identifiers.org/hco/1/GRCh38#201218652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135889729-C-A

201218652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135889729-C-T

201218671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889710-C-T

201218687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889693-G-A

201218687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889693-G-T

201218688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889692-T-G

201218691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889689-A-G

201218694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889686-T-G

201218702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889678-G-A

201218702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889678-G-T

http://identifiers.org/hco/1/GRCh38#201218753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135889640-C-A

201218753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889640-C-G

201218753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889640-C-T

201218853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889549-G-C

http://identifiers.org/hco/1/GRCh38#201219125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135889477-C-A

201219218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889399-G-A

http://identifiers.org/hco/1/GRCh38#201219312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135889306-C-A

201219312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889306-C-T

201219341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889279-A-T

201219352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889267-T-C

201219568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889037-C-G

http://identifiers.org/hco/1/GRCh38#201219608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135889004-C-A

201219608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135889004-C-G

201219736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135888948-G-A

201219837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135888907-T-A

201219837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135888907-T-C

201220649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135888443-C-T

201220727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135888368-G-T

201220939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135888104-T-C

201221081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135887976-A-G

http://identifiers.org/hco/1/GRCh38#201221414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135887772-C-A

201221414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135887772-C-T

201221439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135887745-G-A

201221714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135887469-T-C

http://identifiers.org/hco/1/GRCh38#201221737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135887446-C-A

201221737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135887446-C-G

201221740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135887443-G-T

201221753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135887430-G-A

201221905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135887323-G-T

http://identifiers.org/hco/1/GRCh38#201222026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135887242-A-C

201222026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135887242-A-G

201222026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135887242-A-T

201222098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135887191-G-T

http://identifiers.org/hco/1/GRCh38#201222278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135887074-C-A

201222353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135886994-G-A

201222376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135886971-G-C

201222376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135886971-G-T

201222807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 135886695-C-T

201222856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135886633-G-A

201222856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135886633-G-C

201222856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135886633-G-T

http://identifiers.org/hco/1/GRCh38#201222952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#135886549-C-A

201222952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135886549-C-T

201223087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 135886420-A-G

http://identifiers.org/hco/1/GRCh38#201223105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135886402-C-A

201223123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135886388-C-G

201223123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135886388-C-T

201223138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135886373-T-C

201223202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135886309-G-A

201223202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135886309-G-T

201223994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135886074-T-C

201224027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135886046-C-T

201224039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135886034-G-A

201224191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135885462-G-A

http://identifiers.org/hco/1/GRCh38#201224281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135885364-C-A

201224323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135885324-A-G

201224532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135885144-T-A

201224532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135885144-T-C

201224532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135885144-T-G

http://identifiers.org/hco/1/GRCh38#201224534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135885142-C-A

201224535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135885141-T-A

http://identifiers.org/hco/1/GRCh38#201224568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135885108-C-A

201224568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135885108-C-T

201224712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135884596-G-C

http://identifiers.org/hco/1/GRCh38#201224752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135884556-A-C

http://identifiers.org/hco/1/GRCh38#201224827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135884481-C-A

201224827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135884481-C-T

201224887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135884427-T-C

201224889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135884425-G-T

201224893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135884421-T-C

http://identifiers.org/hco/1/GRCh38#201224939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135884388-C-A

201225109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135884239-G-A

201225109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135884239-G-T

201225207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135884132-T-A

201225315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135884041-G-A

http://identifiers.org/hco/1/GRCh38#201225400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135883972-A-C

201225466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135883928-G-A

201225696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135883760-G-T

201225733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135883727-G-T

201225769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135883708-T-C

http://identifiers.org/hco/1/GRCh38#201225772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135883705-C-A

201225772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135883705-C-T

http://identifiers.org/hco/1/GRCh38#201225818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135883599-C-A

201225841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135883576-G-A

http://identifiers.org/hco/1/GRCh38#201225960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135883457-C-A

201225960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135883457-C-T

http://identifiers.org/hco/1/GRCh38#201225983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135883434-A-C

201225983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135883434-A-G

201225991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135883426-C-T

http://identifiers.org/hco/1/GRCh38#201226009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135883408-C-A

201226009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135883408-C-G

201226130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135883287-A-G

201226544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882902-T-G

201226564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882882-T-C

201226781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882728-G-A

201226781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882728-G-T

201226819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882698-C-G

201226819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882698-C-T

http://identifiers.org/hco/1/GRCh38#201226866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135882651-C-A

201226893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135882621-G-A

201226914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135882600-G-C

201227139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135882375-G-A

201227139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135882375-G-C

201227139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135882375-G-T

201227232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882275-G-A

201227232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882275-G-T

201227244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882264-A-T

201227254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882254-G-A

201227254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882254-G-T

201227255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882253-A-G

http://identifiers.org/hco/1/GRCh38#201227272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135882238-C-A

201227272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882238-C-T

201227274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882236-G-A

201227274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882236-G-T

http://identifiers.org/hco/1/GRCh38#201227283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135882227-C-A

201227283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882227-C-G

201227283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135882227-C-T

201228350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135881812-C-G

201228350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135881812-C-T

201228381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135881778-T-A

201228381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135881778-T-C

http://identifiers.org/hco/1/GRCh38#201228388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135881771-C-A

201228408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 135881729-C-T

201228412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 135881725-C-T

http://identifiers.org/hco/1/GRCh38#201228478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135881647-A-C

201228478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 135881647-A-T

201228551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 135881581-G-A

201228551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 135881581-G-C

201228551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 135881581-G-T

http://identifiers.org/hco/1/GRCh38#201228620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135881520-C-A

201228620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 135881520-C-T

201228676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135881480-T-A

201228676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135881480-T-G

201228710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135881455-G-A

201228710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135881455-G-C

201228710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135881455-G-T

http://identifiers.org/hco/1/GRCh38#201228840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#135881369-A-C

201228840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24607
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 135881369-A-T