http://identifiers.org/hco/3/GRCh38#191267275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27172202-C-A

191267320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172244-A-G

http://identifiers.org/hco/3/GRCh38#191267325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27172249-C-A

191267344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172266-C-G

191267344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172266-C-T

http://identifiers.org/hco/3/GRCh38#191267347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27172269-A-C

191267348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172270-A-G

191267366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172288-T-A

191267366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172288-T-C

191267369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172291-T-C

191267371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172293-A-G

191267380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172302-G-A

http://identifiers.org/hco/3/GRCh38#191267404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27172329-C-A

191267432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172357-A-G

191267449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3 prime UTR variant
orthologous variants: 27172374-A-G

191268362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 27172409-G-T

191268437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 27172483-G-A

191268437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 27172483-G-T

191268470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172512-A-G

http://identifiers.org/hco/3/GRCh38#191268521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27172557-C-A

191268521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172557-C-T

191268549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172587-G-A

http://identifiers.org/hco/3/GRCh38#191268557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27172595-C-A

191268564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172602-G-A

191268564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172602-G-T

191268583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172636-G-A

191268583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172636-G-T

191268584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172637-G-A

191268584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172637-G-C

191268584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172637-G-T

191268692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172742-T-C

191268714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172764-T-C

http://identifiers.org/hco/3/GRCh38#191268748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27172796-A-C

191268783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172830-T-C

191268825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172866-G-A

191268875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 27172928-T-G

191268885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27172938-T-C

191268999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27173047-T-C

191269042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27173091-C-G

191269869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 27173424-T-C

191269896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 27173451-C-T

http://identifiers.org/hco/3/GRCh38#191269957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27173512-C-A

191269982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 27173536-T-A

191269992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 27173546-T-C

191270213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 27173736-C-T

http://identifiers.org/hco/3/GRCh38#191273394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27177656-C-A

191273394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 27177656-C-T

http://identifiers.org/hco/3/GRCh38#191273427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27177688-C-A

191273427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 27177688-C-T

191273460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 27177710-C-T

191273604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27177845-G-A

191273604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27177845-G-T

191273638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27177867-T-C

191273654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27177883-A-G

191273664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27177893-C-G

191273681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27177910-T-C

191273698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27177923-T-A

191273739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27177978-C-G

191273739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27177978-C-T

191274323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27178749-A-T

191274341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27178769-A-G

191274462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27178896-G-A

191274916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27179356-G-A

191274948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27179389-C-T

191275091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27179539-T-C

191275112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27179560-A-G

191275152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27179587-A-G

191275156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27179591-G-A

191275156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27179591-G-T

http://identifiers.org/hco/3/GRCh38#191275178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27179617-C-A

191275178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27179617-C-T

191275238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27179675-A-G

191275245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 27179682-A-G

191275883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27180102-A-G

http://identifiers.org/hco/3/GRCh38#191275894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27180113-C-A

191275894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27180113-C-T

191275901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27180120-T-C

191275908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27180127-G-A

191276121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27180710-G-A

191276143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27180738-T-C

191276144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27180739-A-G

191276427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181371-C-T

191276436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181383-G-C

http://identifiers.org/hco/3/GRCh38#191276462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27181409-C-A

191276502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181455-G-A

191276699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181637-A-G

191276699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181637-A-T

191276728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181663-T-A

191276728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181663-T-C

191276834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 27181762-T-A

191276841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 27181769-A-G

191276865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181792-A-G

191276865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181792-A-T

191276902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181826-T-G

191276974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181883-T-C

191277058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181959-T-C

191277096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27181997-G-A

191277228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27182124-G-A

191277387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27182390-C-G

191277412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27182415-A-G

191277422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27182425-A-G

191277437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27182443-G-A

191277455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27182461-G-T

191277493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 27182498-T-A

191277594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27182573-G-A

191277602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27182581-A-T

191277777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27182718-G-T

191277889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27182827-T-G

191277951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27182891-G-A

191277951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27182891-G-T

http://identifiers.org/hco/3/GRCh38#191277955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27182895-C-A

http://identifiers.org/hco/3/GRCh38#191278046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27183429-A-C

191278046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27183429-A-G

191278046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27183429-A-T

191278091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27183474-G-A

191278091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27183474-G-T

191278113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27183487-A-G

191278614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27183992-G-A

191278635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27184013-A-G

191278653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27184020-G-C

191278653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27184020-G-T

191278698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27184062-T-C

191278716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27184080-C-T

191278825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27184190-G-A

191279069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27184478-T-G

http://identifiers.org/hco/3/GRCh38#191280653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27186947-C-A

191280678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27186977-G-A

191280715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27187015-G-A

191280815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27187116-A-G

191280955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27187269-G-A

191280978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27187292-C-T

191281289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27187609-C-G

191281384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27187700-C-T

191281640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27188366-A-T

http://identifiers.org/hco/3/GRCh38#191281688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27188409-C-A

http://identifiers.org/hco/3/GRCh38#191281781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27188498-C-A

191281988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27188693-A-G

191281988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27188693-A-T

http://identifiers.org/hco/3/GRCh38#191282035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27188735-A-C

191282037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 27188737-T-C

191282181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 27188881-C-G

191282181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 27188881-C-T

http://identifiers.org/hco/3/GRCh38#191282197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27188894-A-C

http://identifiers.org/hco/3/GRCh38#191282266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27188975-C-A

http://identifiers.org/hco/3/GRCh38#191282363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27189056-C-A

191282410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189099-G-A

191282410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189099-G-T

191282421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189110-A-G

191282450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189139-T-A

191282450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189139-T-C

http://identifiers.org/hco/3/GRCh38#191282514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27189204-A-C

191282514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27189204-A-G

191282514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27189204-A-T

http://identifiers.org/hco/3/GRCh38#191282515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27189205-C-A

191282515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27189205-C-G

191282515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27189205-C-T

191282528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27189219-A-T

191282539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27189232-T-A

191282539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27189232-T-C

191282539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27189232-T-G

191282548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189244-G-C

191282548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189244-G-T

191282631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189330-A-G

191282666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189360-A-G

191282686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189376-G-C

191282730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189413-T-G

191283040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189696-C-T

191283056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27189712-G-A

191283530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27190106-G-C

191283789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27190355-T-C

191284146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27190718-C-T

http://identifiers.org/hco/3/GRCh38#191295594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27193276-C-A

http://identifiers.org/hco/3/GRCh38#191295873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27193525-C-A

191295977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27193633-T-C

191296075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27193730-A-G

191296154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27193807-C-T

191296159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27193812-A-G

191296206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27193858-C-T

191296250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27193916-A-G

191296264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27193930-C-T

191296388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27194031-C-T

191296423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27194070-C-T

191296464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27194117-T-A

191296770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27194387-T-C

191296985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27194759-A-G

http://identifiers.org/hco/3/GRCh38#191297339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27195156-C-A

191297417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27195237-T-C

191297474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27195294-G-A

191297516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27195343-C-T

191297620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27195432-C-G

191297739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27195549-T-G

191301337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196032-C-G

191301343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196038-C-T

191301418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196094-T-A

191301418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196094-T-C

191301457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196133-T-C

191301474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196150-T-A

191301474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196150-T-G

191302707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196410-T-C

191306831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196664-C-T

191306851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196684-T-C

191306851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196684-T-G

191306874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196698-C-T

191306875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196699-G-A

191306921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27196744-T-C

191307276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27197046-C-T

191307426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27197192-G-A

191312326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27200842-T-G

191312381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27200897-G-A

191312508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27200985-G-A

191312527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27201005-T-C

191312559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 27201037-T-C

191325693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27202512-T-C

http://identifiers.org/hco/3/GRCh38#191325848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27202802-C-A

191325866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27202820-G-A

191326331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203241-C-T

191326377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203269-G-A

191326377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203269-G-C

191326507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203497-A-G

191326570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203552-A-G

191326702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203670-G-A

191326757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203725-C-T

191326762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203730-C-T

191326844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203801-A-T

191326880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203836-C-T

191326971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203935-A-G

191326985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27203949-G-A

191327076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27204023-T-G

191327092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27204039-T-A

191327092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27204039-T-C

191327625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27206018-A-G

191327739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27206108-C-T

191327762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27206130-G-A

191327956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27206315-T-C

191328302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27206644-A-G

http://identifiers.org/hco/3/GRCh38#191328315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27206664-C-A

191328315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27206664-C-T

191328366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 27206717-T-C

http://identifiers.org/hco/3/GRCh38#191328402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27206751-C-A

191328642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27206989-G-A

191328642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27206989-G-T

191328669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27207014-G-C

191328669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27207014-G-T

191328954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27207419-G-T

http://identifiers.org/hco/3/GRCh38#191329047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27207505-C-A

191329078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 27207535-G-A

191329078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 27207535-G-T

191329128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 27207572-G-T

http://identifiers.org/hco/3/GRCh38#191329171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27207583-C-A

http://identifiers.org/hco/3/GRCh38#191329197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27207609-C-A

191329197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 27207609-C-G

191329197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 27207609-C-T

191329245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 27207620-A-G

191329264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 27207635-G-A

191329264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 27207635-G-T

http://identifiers.org/hco/3/GRCh38#191329291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27207648-A-C

191329291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 27207648-A-G

191329360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27207714-T-A

191329360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 27207714-T-C

http://identifiers.org/hco/3/GRCh38#191329582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27207806-C-A

191329582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27207806-C-G

191329582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 27207806-C-T

191329684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, missense_variant
orthologous variants: 27207848-G-C

http://identifiers.org/hco/3/GRCh38#191329701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27207865-C-A

191329701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 27207865-C-T

http://identifiers.org/hco/3/GRCh38#191329734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27207910-C-A

191329734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, undefined
orthologous variants: 27207910-C-G

191329734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, undefined
orthologous variants: 27207910-C-T

http://identifiers.org/hco/3/GRCh38#191329741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#27207919-A-C

191329741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron_variant, undefined
orthologous variants: 27207919-A-G

191329782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27207945-T-C

http://identifiers.org/hco/3/GRCh38#191329794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27207957-C-A

191329794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27207957-C-T

191329813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27207961-G-A

191329813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27207961-G-C

191329813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27207961-G-T

191329826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27207973-G-A

191329826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27207973-G-C

191329826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27207973-G-T

191330075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27208058-A-G

191330167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27208214-T-C

191330240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27208299-T-A

http://identifiers.org/hco/3/GRCh38#191330285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27208347-C-A

http://identifiers.org/hco/3/GRCh38#191330327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27208376-A-C

191330327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27208376-A-G

191330341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27208390-G-A

191330341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27208390-G-T

191330360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: intron variant
orthologous variants: 27208399-G-T

191330530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27208548-T-C

191330673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27208712-C-T

http://identifiers.org/hco/3/GRCh38#191330711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27208762-C-A

191330711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27208762-C-T

http://identifiers.org/hco/3/GRCh38#191330747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27208798-C-A

191330747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27208798-C-T

191330828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27208876-C-G

191330912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 27208955-G-T

191331080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27209080-G-A

191331195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27209195-G-A

191331359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27209373-C-G

191331378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27209392-T-G

191331451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27209463-C-T

191331764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27209782-T-C

191332063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27210062-G-C

191332096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27210089-G-A

http://identifiers.org/hco/3/GRCh38#191333093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#27210553-A-C

191333345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27210769-G-A

191335632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30894
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 27213051-C-T