http://identifiers.org/hco/3/GRCh38#183707392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19964902-A-C

183707392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19964902-A-G

183710286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 19966085-C-T

183710375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19966234-C-T

183710424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19966247-A-G

http://identifiers.org/hco/3/GRCh38#183710627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19966440-A-C

183710676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19966482-C-T

183710883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19966658-G-A

183711264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19967107-A-G

183711264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19967107-A-T

183711274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19967117-T-C

183711274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19967117-T-G

183714999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19969076-G-A

183714999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19969076-G-T

183715391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19969431-C-G

183717577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19971593-T-A

183717577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19971593-T-C

183718414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19972810-A-T

183718620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19973002-T-C

183721178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19974148-A-G

183721660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19975347-C-T

183721740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19975427-A-G

183721779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19975534-G-C

183721779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19975534-G-T

183722102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: 19975848-A-G

183722114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: 19975860-G-T

183722134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 19975880-A-T

183723059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19976416-T-C

183724423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: 19977891-C-T

183724588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19978061-T-A

http://identifiers.org/hco/3/GRCh38#183724673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19978145-C-A

183724673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19978145-C-G

183724673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19978145-C-T

183727584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19979949-C-G

183728762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 19980798-C-T

183732314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986243-C-T

http://identifiers.org/hco/3/GRCh38#183732407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19986310-C-A

183732557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986446-A-G

183732557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986446-A-T

183732646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986539-G-A

183732652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986545-C-T

183732690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986567-A-G

http://identifiers.org/hco/3/GRCh38#183732691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19986568-C-A

183732704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986581-C-T

183732705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986582-G-A

183732709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986586-G-A

http://identifiers.org/hco/3/GRCh38#183732725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19986656-A-C

183732839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986831-G-A

183732839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19986831-G-C

183733006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19987103-G-A

183733016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19987116-T-C

183733137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19987243-A-G

http://identifiers.org/hco/3/GRCh38#183733331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19987536-A-C

183733482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19987654-C-T

183733639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19987814-C-T

183734226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19988180-C-T

183734494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19988439-A-G

183734534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19988480-T-A

183735549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19989060-T-C

183735604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19989109-A-G

183735604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19989109-A-T

183735868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19989205-C-G

183736401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19989650-T-C

183736478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19989719-A-G

http://identifiers.org/hco/3/GRCh38#183736567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19989801-A-C

183736686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19989908-G-A

183736702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19989925-A-G

183743944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19991187-G-A

183746833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19992536-G-A

183746851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19992554-C-T

183747059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19992758-T-C

183747660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19993233-G-A

183747660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19993233-G-T

183751723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19998006-A-G

http://identifiers.org/hco/3/GRCh38#183751730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19998013-A-C

183751730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19998013-A-G

183751764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19998042-A-G

183751984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19998172-A-G

http://identifiers.org/hco/3/GRCh38#183752007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19998190-C-A

183752007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19998190-C-G

183752007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19998190-C-T

183752013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19998196-T-G

183752087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 19998265-A-T

183752108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 19998286-A-G

183752116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 19998294-G-A

183752132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 19998310-C-T

183752187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 19998362-C-G

183752187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 19998362-C-T

183752205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 19998377-C-G

183752205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 19998377-C-T

http://identifiers.org/hco/3/GRCh38#183752228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#19998400-A-C

183752228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 19998400-A-G

183752246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 19998418-G-A

183752249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 19998421-G-A

183752264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 19998433-A-T

183754067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20004948-G-A

183754067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20004948-G-T

183754078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20004956-T-C

183754083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20004961-A-G

183754138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 20005013-G-A

183754157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 20005032-C-G

183754223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20005098-A-G

183754310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20005185-T-C

http://identifiers.org/hco/3/GRCh38#183754430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20005338-A-C

183754435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20005344-A-G

183754439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20005348-T-C

183754511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20005467-T-C

183754513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20005469-G-A

183754513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20005469-G-T

183754514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20005470-G-A

183754514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20005470-G-T

183754517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20005473-A-T

183754885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20005754-G-A

183755709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20006488-G-T

http://identifiers.org/hco/3/GRCh38#183756550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20008111-C-A

183756550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20008111-C-T

183756620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: 20008181-A-G

183756799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20008328-A-G

183757742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20008616-A-G

183758837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20009111-G-A

183758917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20009191-C-T

183758985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20009258-A-G

http://identifiers.org/hco/3/GRCh38#183758991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20009264-C-A

183758991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20009264-C-T

http://identifiers.org/hco/3/GRCh38#183760553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20010506-C-A

183760575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20010526-G-A

183760689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20010581-G-C

183760794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20010690-G-A

183760919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20010810-A-G

183760969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20011521-A-T

183760970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20011522-C-T

183761422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20011821-A-G

183761422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20011821-A-T

183761503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 20011905-A-G

183761636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012038-G-C

http://identifiers.org/hco/3/GRCh38#183761745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20012089-A-C

183761745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012089-A-G

183761894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012219-G-C

183761988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012295-G-A

http://identifiers.org/hco/3/GRCh38#183762009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20012307-C-A

183762009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012307-C-G

183762039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012327-G-C

183762348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012648-G-A

183762348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012648-G-T

183762409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012709-G-A

183762409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012709-G-T

http://identifiers.org/hco/3/GRCh38#183762420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20012722-A-C

183762420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012722-A-G

183762429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012731-G-A

183762429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012731-G-T

183762474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012782-C-T

183762634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012925-G-A

183762657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20012948-G-T

183763457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20013146-T-C

183763488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20013171-G-A

183763631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20013362-G-A

183771420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20021595-T-C

183772337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20022437-T-C

183772553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20022653-C-T

183772628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20022697-G-A

183772628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20022697-G-C

183772699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20022747-G-T

http://identifiers.org/hco/3/GRCh38#183773409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20024660-A-C

183773562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20024766-T-C

183773892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20025087-T-C

183773915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20025110-G-A

183773915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20025110-G-T

183773920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20025115-G-A

183773920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20025115-G-T

183776188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20026607-T-C

183776188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20026607-T-G

183777117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20026881-G-T

183777432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20027091-G-T

183777458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20027101-G-A

183777465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20027111-G-C

183777488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20027122-C-G

183777637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20027264-T-A

183777707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 20027334-A-T

http://identifiers.org/hco/3/GRCh38#183777723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20027350-C-A

183777723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20027350-C-T

183786163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20028820-C-G

183786163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20028820-C-T

183786193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20028850-C-G

183786623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20029308-T-G

183786704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20029480-T-G

183786717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20029494-T-G

183786721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20029498-T-A

183786780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20029559-G-A

183786954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20029690-A-G

183790735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20030260-C-T

183790747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20030273-A-G

183790752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20030278-G-A

183790752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20030278-G-T

http://identifiers.org/hco/3/GRCh38#183790777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20030303-C-A

183790777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20030303-C-T

http://identifiers.org/hco/3/GRCh38#183790832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20030351-C-A

183790859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20030378-G-A

183790859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: 20030378-G-C

183790905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: 20030424-G-A

183790907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20030426-C-T

183790914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: 20030433-A-G

183790914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: 20030433-A-T

http://identifiers.org/hco/3/GRCh38#183790915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20030434-C-A

http://identifiers.org/hco/3/GRCh38#183790916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20030435-C-A

183790916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20030435-C-T

183790921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense variant
orthologous variants: 20030440-T-C

183790931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20030450-G-A

183790931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20030450-G-T

183791031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20030544-A-T

183797694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20031710-C-T

183797715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20031731-C-G

http://identifiers.org/hco/3/GRCh38#183797820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20031920-C-A

183797862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron variant
orthologous variants: 20031962-A-G

183797942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: synonymous variant
orthologous variants: 20032036-C-T

183798118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20032201-G-A

183798319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20032452-T-C

183798335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20032465-C-G

183799042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033287-G-T

http://identifiers.org/hco/3/GRCh38#183799073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20033320-C-A

183799073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033320-C-G

183799073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033320-C-T

183799079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033326-G-C

183799081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033327-G-A

183799081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033327-G-T

183799125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033408-G-A

183799125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033408-G-T

http://identifiers.org/hco/3/GRCh38#183799159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20033449-C-A

183799159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033449-C-T

183799177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033471-T-C

183799401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033794-T-C

183799423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20033817-C-G

183799736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20036831-A-G

183800261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20036962-G-C

183800374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037060-T-C

183800374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037060-T-G

183800377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037063-G-T

http://identifiers.org/hco/3/GRCh38#183800422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20037093-C-A

183800423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037094-A-T

http://identifiers.org/hco/3/GRCh38#183800424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20037095-C-A

http://identifiers.org/hco/3/GRCh38#183800429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20037099-C-A

183800429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037099-C-T

183800585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037253-T-G

183800610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037277-G-A

http://identifiers.org/hco/3/GRCh38#183800630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20037307-C-A

183800656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037386-G-A

183800656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037386-G-T

183800672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037430-G-A

183800672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037430-G-T

183800695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037467-G-A

183800695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037467-G-C

183800695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037467-G-T

183800706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037498-A-G

183800843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037655-T-C

http://identifiers.org/hco/3/GRCh38#183800899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20037704-C-A

183800899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037704-C-T

http://identifiers.org/hco/3/GRCh38#183800903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20037706-C-A

183800903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037706-C-T

http://identifiers.org/hco/3/GRCh38#183800934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20037738-A-C

183800934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037738-A-G

183800946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037753-T-A

183800946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037753-T-C

183800972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037766-C-G

183800972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20037766-C-T

http://identifiers.org/hco/3/GRCh38#183801103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20037888-C-A

183801103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20037888-C-T

183801485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20038398-C-G

http://identifiers.org/hco/3/GRCh38#183801540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20038452-A-C

183801557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20038462-G-A

183801557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20038462-G-T

http://identifiers.org/hco/3/GRCh38#183801570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20038470-C-A

183801886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20038762-G-T

http://identifiers.org/hco/3/GRCh38#183801985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20038839-C-A

183801985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20038839-C-T

183802071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20038915-G-C

183802094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20038941-T-C

183802501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20039527-G-A

183802507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20039541-G-A

183802585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20039634-A-G

183802780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20039896-A-G

183802798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20039926-T-A

183802798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20039926-T-C

183802798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20039926-T-G

183802836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20039963-A-G

183802836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20039963-A-T

http://identifiers.org/hco/3/GRCh38#183802842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20039969-A-C

183802842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20039969-A-G

http://identifiers.org/hco/3/GRCh38#183803350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20040578-C-A

183803373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20040642-G-A

183803373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20040642-G-T

183803376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20040645-A-G

183803433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20040742-G-A

183803433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20040742-G-T

http://identifiers.org/hco/3/GRCh38#183803496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20040856-C-A

183803496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20040856-C-G

183803496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20040856-C-T

183803522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20040899-G-A

183803522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20040899-G-T

183803674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20041051-G-A

183803674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20041051-G-T

183803787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20041136-A-G

183803787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20041136-A-T

183803822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20041171-G-C

183803822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 20041171-G-T

183804052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20041555-C-T

http://identifiers.org/hco/3/GRCh38#183804142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20041645-C-A

183804142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 20041645-C-T

183804199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20041702-A-G

183805902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20042251-G-T

183806490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046157-G-A

http://identifiers.org/hco/3/GRCh38#183806516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20046179-C-A

http://identifiers.org/hco/3/GRCh38#183806534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20046198-C-A

183806590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046253-G-A

183806590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046253-G-C

183806590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046253-G-T

183806614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046277-G-T

http://identifiers.org/hco/3/GRCh38#183806615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20046278-A-C

183806615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046278-A-G

183806615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046278-A-T

183806640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046302-T-C

183806750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046371-G-A

183806750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046371-G-T

183807103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046707-T-C

http://identifiers.org/hco/3/GRCh38#183807167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20046747-A-C

183807167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046747-A-G

183807347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046840-G-A

183807347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046840-G-T

183807364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046857-C-G

183807367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046860-G-C

183807367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20046860-G-T

183807549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047026-A-G

183807563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047040-A-G

http://identifiers.org/hco/3/GRCh38#183807634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20047113-A-C

183807634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047113-A-G

183807693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047201-A-G

183807701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047209-G-A

183807701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047209-G-T

183807783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047258-G-A

183807783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047258-G-T

183807841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047301-G-A

http://identifiers.org/hco/3/GRCh38#183807848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20047308-C-A

183807853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047313-T-C

http://identifiers.org/hco/3/GRCh38#183807905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20047326-A-C

183807905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047326-A-G

http://identifiers.org/hco/3/GRCh38#183807915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20047336-C-A

183807915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047336-C-T

http://identifiers.org/hco/3/GRCh38#183808134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20047551-A-C

183808138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047555-A-T

http://identifiers.org/hco/3/GRCh38#183808150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20047568-C-A

183808159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20047576-T-G

http://identifiers.org/hco/3/GRCh38#183808262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20047669-C-A

183808262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20047669-C-T

183808281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20047684-A-T

183809274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20048406-G-T

183809275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20048407-G-T

http://identifiers.org/hco/3/GRCh38#183809466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20048556-A-C

183809466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20048556-A-T

183809728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20048790-A-T

183809948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20048970-T-C

http://identifiers.org/hco/3/GRCh38#183810072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20049108-C-A

183810072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20049108-C-T

183810116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20049148-T-G

http://identifiers.org/hco/3/GRCh38#183810131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20049160-A-C

183810190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20049217-C-T

183810285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20049276-G-T

183810396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20049406-T-A

183810396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20049406-T-C

http://identifiers.org/hco/3/GRCh38#183810430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20049442-C-A

183810430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20049442-C-T

183810453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20049466-C-T

http://identifiers.org/hco/3/GRCh38#183810457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20049497-C-A

http://identifiers.org/hco/3/GRCh38#183810649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20049689-C-A

183810649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049689-C-T

183810688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049725-G-T

183810742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049779-G-A

183810742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049779-G-T

http://identifiers.org/hco/3/GRCh38#183810857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20049887-C-A

183810857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049887-C-G

183810857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049887-C-T

183810903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049941-G-A

183810903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049941-G-T

http://identifiers.org/hco/3/GRCh38#183810972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20049992-C-A

183810972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049992-C-T

183810974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049994-T-A

183810974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20049994-T-C

183811060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050046-G-A

183811064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050050-G-A

183811064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050050-G-T

183811132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050112-G-C

183811132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050112-G-T

183811191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050165-G-A

183811191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050165-G-T

http://identifiers.org/hco/3/GRCh38#183811689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20050549-C-A

183811689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050549-C-T

183811827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050678-G-A

183811852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050707-G-A

183811852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050707-G-T

183811884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050743-G-T

183812092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050894-G-A

183812092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050894-G-T

183812127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20050928-C-T

http://identifiers.org/hco/3/GRCh38#183812217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#20051006-C-A

183812235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20051025-A-G

183812354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25489
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 20051071-A-G