http://identifiers.org/hco/2/GRCh38#25042078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4088943-C-A

25042078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 4088943-C-G

25042078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 4088943-C-T

http://identifiers.org/hco/2/GRCh38#25042141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4088880-C-A

25042141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 4088880-C-G

25042141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 4088880-C-T

25042210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5 prime UTR variant
orthologous variants: 4088809-G-A

25042210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5 prime UTR variant
orthologous variants: 4088809-G-C

25042210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5 prime UTR variant
orthologous variants: 4088809-G-T

25042220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5 prime UTR variant
orthologous variants: 4088799-G-A

25042220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5 prime UTR variant
orthologous variants: 4088799-G-C

25042220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5 prime UTR variant
orthologous variants: 4088799-G-T

http://identifiers.org/hco/2/GRCh38#25042241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4088779-C-A

25042241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5 prime UTR variant
orthologous variants: 4088779-C-G

25042241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5 prime UTR variant
orthologous variants: 4088779-C-T

25042325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4088696-G-A

25042325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4088696-G-C

25042325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4088696-G-T

25042379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4088657-G-A

25042471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088566-G-A

25042471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088566-G-T

25042479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088558-G-A

25042479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088558-G-T

25042531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088498-C-G

25042531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088498-C-T

25042608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088394-A-G

25042615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088391-G-C

25042615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088391-G-T

25042643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088363-G-A

25042643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4088363-G-T

25042707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4088300-C-T

25042786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4088220-G-A

http://identifiers.org/hco/2/GRCh38#25043198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4087865-C-A

25043319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4087748-G-A

25043571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4087531-C-G

25044575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4086529-G-A

25045063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4085991-G-T

25045324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4085620-C-T

http://identifiers.org/hco/2/GRCh38#25046635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4084590-C-A

25053457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4080647-C-T

25055661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4080027-C-T

25056119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4079368-G-A

25056119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4079368-G-C

25056515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4078989-C-T

25056768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4078769-G-A

25056768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4078769-G-T

25056919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4078606-T-C

25057037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4078457-C-T

25062094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4075060-A-T

25062323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4074861-G-A

25062544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4074657-G-A

http://identifiers.org/hco/2/GRCh38#25062581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4074620-C-A

25062657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4074532-C-T

25062662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4074526-T-C

25062664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4074524-G-A

25062664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4074524-G-C

25062838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4074375-A-G

25063662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4073884-A-G

25063730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4073805-T-C

25063749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4073786-C-T

25063965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4073608-T-C

25064143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4073237-C-T

25064271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4073106-C-T

25064451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4072920-G-A

25064461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4072910-G-A

25064655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4072676-A-G

25064708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4072458-A-G

25066569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4070727-C-T

25066736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4070568-A-G

25066893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4070402-T-C

25072504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4065962-A-G

25072680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4065869-C-G

25072808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4065775-A-G

http://identifiers.org/hco/2/GRCh38#25072900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4065684-C-A

25073066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4065519-T-C

25073241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4065380-G-A

25073389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4065258-G-A

25073389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4065258-G-T

25074191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4064189-G-A

25074970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4063095-G-T

25075072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4063013-G-T

25075137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4062948-A-G

25075319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4062734-T-G

25075325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4062728-C-T

25075897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4061794-C-T

25076505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4059351-A-T

25076533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4059304-G-T

25076640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4059196-T-C

25076854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4058976-C-T

25077082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4058750-C-T

25077198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4058634-T-A

25077549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4058539-A-G

25077553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4058535-T-C

25077817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4058339-G-A

25077959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4058249-C-T

25078250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4057948-T-C

25078349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4057842-A-G

25078553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4057643-A-G

25078629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4057559-G-A

25078783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4057362-C-G

25079243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4056963-A-G

25079366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4056846-T-C

25079391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4056822-T-C

25079410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4056801-A-G

25081754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4056665-A-G

25081917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4056493-G-A

25081981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4056434-G-T

25082037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4056361-C-T

25090152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054963-T-C

http://identifiers.org/hco/2/GRCh38#25090207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4054908-A-C

25090247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054873-G-A

25090247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054873-G-T

25090260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054869-A-G

25090395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054715-G-C

25090416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054706-G-A

25090500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054623-A-G

25090675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054473-C-T

25090732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054421-T-C

25090791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054376-G-A

25090824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054345-C-T

25090857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4054318-G-A

25090900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4051290-G-A

25091004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4051198-T-G

25091063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4051132-A-G

25091185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4051056-C-T

25091277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4051003-G-T

25091460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050864-G-A

25091460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050864-G-T

25091463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050861-G-A

25091463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050861-G-C

25091548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050812-G-T

25091658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050728-C-T

http://identifiers.org/hco/2/GRCh38#25091740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4050665-C-A

http://identifiers.org/hco/2/GRCh38#25091752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4050653-C-A

25091877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050543-C-T

25091977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050458-T-C

25092101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050369-G-A

25092101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050369-G-T

25092206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050307-T-C

25092417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4050161-C-T

http://identifiers.org/hco/2/GRCh38#25092890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4049836-C-A

http://identifiers.org/hco/2/GRCh38#25092895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4049831-A-C

25092918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049807-T-G

25092968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049751-T-A

25093007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 4049711-G-A

25093007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 4049711-G-C

25093177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049539-G-A

25093177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049539-G-T

http://identifiers.org/hco/2/GRCh38#25093191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4049521-A-C

25093191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049521-A-T

25093201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049511-T-A

25093712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049320-G-A

25093927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049189-A-G

25094027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049168-C-G

25094240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049047-G-A

25094256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049031-G-T

25094274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049016-G-A

25094274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4049016-G-T

25094332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4048930-G-A

25094579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4048709-G-T

http://identifiers.org/hco/2/GRCh38#25096953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4046961-A-C

25097202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4046714-T-G

25097410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4046526-T-G

25097483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4046458-T-C

25097553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4046410-G-A

25097643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4046328-T-G

25097785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4046220-C-G

25097968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4046052-G-A

25098125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4045915-C-T

25098304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4045587-G-T

25098344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4045554-G-A

25098514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4045015-G-T

25099105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4044691-C-T

http://identifiers.org/hco/2/GRCh38#25099196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4044586-C-A

25099196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4044586-C-T

25099391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4044443-G-T

25103477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4043179-C-T

http://identifiers.org/hco/2/GRCh38#25103488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4043168-A-C

25103489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4043167-A-G

25103505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4043151-G-T

25103516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4043140-G-A

25103516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4043140-G-T

25103521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4043135-G-A

http://identifiers.org/hco/2/GRCh38#25103532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4043124-C-A

25103532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4043124-C-T

http://identifiers.org/hco/2/GRCh38#25103571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4043104-C-A

25103571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4043104-C-T

25104221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4042296-G-A

25104549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4042067-A-G

25104940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4041710-T-A

25105274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4041508-T-C

25105291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4041491-T-C

25105462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4041419-T-A

25105677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4041216-T-C

25105901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4041021-C-T

25105930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4041003-T-C

25105949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4040991-G-A

25112757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4040409-C-G

25112757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4040409-C-T

25112871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4040295-G-A

25112902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4040264-G-A

25112945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4040199-A-T

25112950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4040194-G-A

25119477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: -G-A

25119498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: -C-T

25119546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: -T-C

25119580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: -T-C

25119781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4036727-C-T

25120800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4035990-C-T

25120801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4035989-A-G

25121627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4035589-T-C

25121643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4035577-T-C

25121830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4035394-T-A

25121830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4035394-T-C

25121830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4035394-T-G

http://identifiers.org/hco/2/GRCh38#25121832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4035392-C-A

25121832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4035392-C-T

25121875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4035352-C-T

25121932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4035302-G-A

25128157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4034707-G-A

25128292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: missense variant
orthologous variants: 4034572-T-G

25128355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4034513-G-A

25128355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4034513-G-C

http://identifiers.org/hco/2/GRCh38#25128358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4034510-C-A

25128358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4034510-C-T

25128654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4034257-G-A

http://identifiers.org/hco/2/GRCh38#25129007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#4034243-C-A

25129256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4034015-T-C

25129256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4034015-T-G

25129391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron_variant, undefined
orthologous variants: 4033936-C-T

25129423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4033904-A-G

25129925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4033567-T-C

25130048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: missense variant
orthologous variants: 4033443-C-T

25130142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4033323-C-G

25130152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4033313-G-T

25130153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4033312-G-A

http://identifiers.org/hco/2/GRCh38#25130183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4033285-C-A

25130193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4033275-G-A

25130196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4033272-A-G

25130196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4033272-A-T

25130699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4032790-A-G

http://identifiers.org/hco/2/GRCh38#25130726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4032765-C-A

25130726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4032765-C-G

http://identifiers.org/hco/2/GRCh38#25130781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4032691-A-C

25130789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4032683-C-G

25131035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4032453-A-G

25131260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4032219-T-G

http://identifiers.org/hco/2/GRCh38#25131282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4032197-C-A

25131282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4032197-C-T

25131314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4032164-G-A

25131314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4032164-G-T

http://identifiers.org/hco/2/GRCh38#25131325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4032153-C-A

25131416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: missense variant
orthologous variants: 4032055-G-A

25131574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4031942-A-G

25131590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4031932-G-A

25131590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4031932-G-C

25131591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4031931-G-A

25131966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4031474-G-A

25131966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4031474-G-C

25131966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4031474-G-T

http://identifiers.org/hco/2/GRCh38#25131983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4031405-A-C

25131983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4031405-A-G

25132130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4031173-A-G

25132273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4031023-A-T

25132332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4030967-C-T

http://identifiers.org/hco/2/GRCh38#25132624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4030800-A-C

25132638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4030786-C-G

http://identifiers.org/hco/2/GRCh38#25132647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4030777-A-C

25132665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4030763-T-C

25132701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4030736-C-T

http://identifiers.org/hco/2/GRCh38#25132824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4030616-C-A

http://identifiers.org/hco/2/GRCh38#25132879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4030583-C-A

25132881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4030581-C-T

25133037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4030425-C-G

25133037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4030425-C-T

http://identifiers.org/hco/2/GRCh38#25133191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4030313-C-A

25133384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 4030190-G-A

http://identifiers.org/hco/2/GRCh38#25133399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4030175-C-A

25133645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4029972-A-G

25133737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4029880-C-T

25133845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4029807-C-G

25133845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4029807-C-T

25134010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4029656-G-A

25134180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4029293-T-A

http://identifiers.org/hco/2/GRCh38#25134808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4028689-A-C

25134918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4028533-G-A

25135127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4028375-G-A

25135330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4028229-G-A

25135330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4028229-G-T

25135404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4028155-A-G

25135404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4028155-A-T

http://identifiers.org/hco/2/GRCh38#25135452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4028097-A-C

25135452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4028097-A-G

http://identifiers.org/hco/2/GRCh38#25135704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4027857-C-A

http://identifiers.org/hco/2/GRCh38#25135718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4027841-C-A

25135755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4027827-T-C

25135934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4027668-T-G

http://identifiers.org/hco/2/GRCh38#25136435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4027276-C-A

http://identifiers.org/hco/2/GRCh38#25137235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4026960-C-A

25137235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4026960-C-T

http://identifiers.org/hco/2/GRCh38#25137246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4026949-C-A

http://identifiers.org/hco/2/GRCh38#25137254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4026942-C-A

25137254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4026942-C-G

http://identifiers.org/hco/2/GRCh38#25137280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4026916-C-A

25137311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4026895-C-T

http://identifiers.org/hco/2/GRCh38#25137313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4026893-C-A

25137313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4026893-C-T

25137404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: missense variant
orthologous variants: 4026811-C-T

25137518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4026697-C-T

25137636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4026590-G-A

25137636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4026590-G-T

http://identifiers.org/hco/2/GRCh38#25137648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4026582-C-A

25137747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4026490-G-T

25137840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4026396-C-T

25138005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4026316-C-T

25138692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4025797-A-G

25138776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4025730-C-T

25138978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4025542-G-C

25138978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4025542-G-T

25140516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4024178-A-G

25141202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4023840-T-A

25141216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4023826-A-G

25141216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4023826-A-T

25141294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4023753-G-A

25141294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4023753-G-T

http://identifiers.org/hco/2/GRCh38#25141345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4023694-C-A

25141345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4023694-C-G

25141709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4022995-G-A

25143714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4021912-T-A

25143734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: splice acceptor variant
orthologous variants: 4021892-G-A

http://identifiers.org/hco/2/GRCh38#25143763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4021863-A-C

25143763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: missense variant
orthologous variants: 4021863-A-G

http://identifiers.org/hco/2/GRCh38#25143938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4021693-C-A

25143938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4021693-C-T

25143987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4021640-G-A

25144766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4021235-C-G

25144809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4021191-T-C

25144849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4021151-T-C

25144896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4021128-T-C

http://identifiers.org/hco/2/GRCh38#25145122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4020934-C-A

25145122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020934-C-G

http://identifiers.org/hco/2/GRCh38#25145129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4020927-C-A

25145133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020923-G-A

25145133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020923-G-T

25145174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020883-T-A

25145174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020883-T-C

http://identifiers.org/hco/2/GRCh38#25145205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4020852-C-A

25145205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020852-C-T

25145226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020831-G-A

25145226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020831-G-T

http://identifiers.org/hco/2/GRCh38#25146110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4020725-A-C

25146110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020725-A-T

25146136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020698-A-G

25146137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020697-G-A

25146426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020516-G-A

25146457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020486-G-A

http://identifiers.org/hco/2/GRCh38#25146502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4020441-C-A

http://identifiers.org/hco/2/GRCh38#25146507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4020436-C-A

25146507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020436-C-T

25146508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020435-G-A

25146508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020435-G-T

25146528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020416-G-T

http://identifiers.org/hco/2/GRCh38#25146661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4020294-C-A

25146718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020246-G-T

25146794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020189-T-A

25146794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 4020189-T-C

25149747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4019558-G-A

25149782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4019519-G-A

25149782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4019519-G-C

25149782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4019519-G-T

25149783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4019518-G-C

http://identifiers.org/hco/2/GRCh38#25149792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4019513-C-A

25149792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4019513-C-G

25149792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4019513-C-T

25151634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4018854-G-A

25151635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4018853-G-A

25151635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4018853-G-C

http://identifiers.org/hco/2/GRCh38#25151833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4018703-A-C

25151903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4018642-C-G

25151903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4018642-C-T

25152003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: missense variant
orthologous variants: 4018542-G-A

25152090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4018459-T-C

25152110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4018444-G-A

25152110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4018444-G-T

http://identifiers.org/hco/2/GRCh38#25152143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4018434-C-A

http://identifiers.org/hco/2/GRCh38#25152156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4018422-A-C

25152220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4018372-C-T

25152221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4018371-G-A

25153474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4017440-C-T

25153573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4017283-A-G

25153700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4017162-G-A

http://identifiers.org/hco/2/GRCh38#25153772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4017090-A-C

25153772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4017090-A-T

http://identifiers.org/hco/2/GRCh38#25153773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4017089-C-A

25153773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4017089-C-T

http://identifiers.org/hco/2/GRCh38#25153852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4017024-C-A

25153852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4017024-C-T

25154070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4016691-T-C

http://identifiers.org/hco/2/GRCh38#25154104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4016657-C-A

25154104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4016657-C-T

25154220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: intron variant
orthologous variants: 4016555-G-A

25154281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: missense variant
orthologous variants: 4016499-C-T

25154354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4016426-G-A

25154354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4016426-G-C

25154478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4016320-A-T

http://identifiers.org/hco/2/GRCh38#25154521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4016280-C-A

25154540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4016261-G-A

25154540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4016261-G-T

25154613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4016182-G-A

25154613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4016182-G-T

25154691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4016105-A-G

25154761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4016029-G-T

25154804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4016008-T-C

25154950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015878-G-A

25154950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015878-G-T

http://identifiers.org/hco/2/GRCh38#25154953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4015875-A-C

25154953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015875-A-G

25154953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015875-A-T

25154988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015830-T-A

25154988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015830-T-C

http://identifiers.org/hco/2/GRCh38#25155023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4015783-C-A

http://identifiers.org/hco/2/GRCh38#25155073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4015733-C-A

25155073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015733-C-T

http://identifiers.org/hco/2/GRCh38#25155180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4015644-C-A

25155196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015623-T-C

25155220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015584-A-T

25155239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015565-C-T

25155268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015536-G-T

25155401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015439-T-C

25155443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015397-G-T

25155521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015324-T-C

http://identifiers.org/hco/2/GRCh38#25155616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4015234-C-A

25155616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015234-C-T

25155628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015222-T-C

25155894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015042-T-C

25155900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4015036-A-G

25155932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014984-T-G

25156141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014769-G-A

25156142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014768-A-G

25156142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014768-A-T

http://identifiers.org/hco/2/GRCh38#25156150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4014760-C-A

25156150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014760-C-T

http://identifiers.org/hco/2/GRCh38#25156160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4014750-C-A

25156160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014750-C-T

http://identifiers.org/hco/2/GRCh38#25156673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4014565-C-A

25156838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014455-A-G

http://identifiers.org/hco/2/GRCh38#25156864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4014431-C-A

http://identifiers.org/hco/2/GRCh38#25156880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4014415-C-A

25156992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014316-G-A

25156992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014316-G-T

25157097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014210-A-G

http://identifiers.org/hco/2/GRCh38#25157141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4014175-C-A

25157141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014175-C-T

25157163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014152-T-C

25157204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014111-G-A

25157204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014111-G-T

25157216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4014104-G-T

25157336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013977-T-C

http://identifiers.org/hco/2/GRCh38#25157496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4013860-C-A

http://identifiers.org/hco/2/GRCh38#25157514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4013842-C-A

25157514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013842-C-G

25157559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013797-C-T

25157626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013728-G-A

25157641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013713-G-A

25157641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013713-G-T

http://identifiers.org/hco/2/GRCh38#25157782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4013603-C-A

25157782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013603-C-T

http://identifiers.org/hco/2/GRCh38#25157783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4013602-C-A

25157929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013505-A-G

25157930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013504-T-C

25158078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013369-T-A

25158191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013261-G-T

http://identifiers.org/hco/2/GRCh38#25158287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4013203-C-A

25158287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013203-C-G

http://identifiers.org/hco/2/GRCh38#25158345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4013153-C-A

25158345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013153-C-T

25158348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013150-G-T

25158365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013136-T-C

25158408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013096-G-T

http://identifiers.org/hco/2/GRCh38#25158432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4013069-A-C

25158432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013069-A-G

25158432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4013069-A-T

25158538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012998-G-A

25158690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012956-A-G

25158704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012942-T-C

25158708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012938-G-A

25158708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012938-G-T

25158711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012935-G-A

25158711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012935-G-T

25158834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012820-C-T

http://identifiers.org/hco/2/GRCh38#25158946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#4012692-C-A

25158946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012692-C-T

25158960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012678-C-T

25159105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29155
most severe consequence: 3 prime UTR variant
orthologous variants: 4012584-C-T