http://identifiers.org/hco/5/GRCh38#121961976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52598761-C-A

121961976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 52598761-C-G

121961976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 52598761-C-T

121961981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 52598766-T-A

121961981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 52598766-T-C

121961981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 52598766-T-G

121962002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 52598791-G-A

121962037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52598826-C-T

http://identifiers.org/hco/5/GRCh38#121962159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52598934-C-A

121962159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52598934-C-G

121962159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52598934-C-T

121962183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52598939-G-A

121962183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52598939-G-T

121962225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52598969-A-T

121962245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: 52598980-G-C

121962307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52599033-G-C

121962318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: 52599042-C-G

121962428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52599158-A-G

121962649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52599346-C-T

121962758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52599441-C-T

121962768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52599444-A-G

http://identifiers.org/hco/5/GRCh38#121962847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52599542-C-A

121962847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52599542-C-G

121962847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52599542-C-T

121962886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52599589-C-T

121962911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52599620-A-G

121963018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52599691-C-T

http://identifiers.org/hco/5/GRCh38#121963354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52600114-C-A

121963354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52600114-C-T

121963457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52600551-G-A

121963461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52600555-C-T

121963488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52600581-G-A

121963500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52600594-A-G

121963501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52600595-G-C

121963512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52600606-A-T

121963612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52600703-A-G

121963696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52600752-C-G

121963829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52600888-A-G

121966359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52603141-A-T

121966475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52603250-G-A

121966567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52603335-A-G

121966575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52603343-C-G

http://identifiers.org/hco/5/GRCh38#121966680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52603441-C-A

121966699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52603458-A-G

121966801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52603603-A-T

121967342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604168-G-A

121967342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604168-G-C

121967342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604168-G-T

121967345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604171-A-G

http://identifiers.org/hco/5/GRCh38#121967350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52604178-C-A

121967356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604202-G-T

121967865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604413-T-C

121968039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604575-T-C

121968080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604608-G-C

121968099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604625-A-G

121968637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604736-G-A

121968829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604888-T-C

121968968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52604988-A-G

121969103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: 52605102-T-C

121969126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52605122-A-G

121969267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: 52605259-A-G

http://identifiers.org/hco/5/GRCh38#121969296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52605286-A-C

121969447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: 52605356-C-T

121969452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: 52605361-G-A

121969511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: 52605417-T-G

http://identifiers.org/hco/5/GRCh38#121969521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52605427-A-C

121969521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: 52605427-A-G

121969569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: 52605466-T-A

121969831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52605655-C-T

121969832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52605656-T-G

121970292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607389-G-A

121970319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607416-A-G

121970322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607419-G-C

121970378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607480-A-G

121970558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607715-G-T

121970567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607743-G-A

121970590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607794-G-A

121970590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607794-G-T

121970611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607812-G-A

121970611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607812-G-T

121970674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607878-G-T

121970712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607921-A-G

121970795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607979-G-A

121970795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607979-G-C

121970797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607981-G-A

121970805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52607989-G-T

121970958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608134-A-G

http://identifiers.org/hco/5/GRCh38#121971076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52608237-C-A

http://identifiers.org/hco/5/GRCh38#121973886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52608385-A-C

121973895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608394-T-C

121974017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608510-T-C

121974140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608617-T-C

121974147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608624-G-T

121974148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608625-T-C

121974156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608633-G-T

121974159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608636-A-G

121974159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608636-A-T

121974252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52608724-T-C

121974252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52608724-T-G

121974255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52608727-C-T

121974271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52608743-C-G

121974316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608788-A-G

http://identifiers.org/hco/5/GRCh38#121974348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52608811-C-A

121974348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608811-C-G

121974353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608816-A-G

121974423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608870-T-A

121974428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52608871-T-G

121974613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609054-A-G

121974698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609135-G-A

121974757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609191-A-G

121975318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52609375-T-C

121975426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609476-G-C

121975428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609478-G-A

121975448-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609493-T-A

121975491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609531-G-C

121975491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609531-G-T

121975505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609546-G-A

121975505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609546-G-T

121975514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609555-T-C

121975515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609556-G-A

121975779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609819-G-T

121975905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52609939-A-G

121976000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52610033-C-T

121976132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52610163-C-T

121977214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, undefined
orthologous variants: 52610659-T-A

http://identifiers.org/hco/5/GRCh38#121977280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52610720-A-C

121977400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52610867-A-G

121977532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52610990-G-A

121977532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52610990-G-T

121977834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611284-A-T

121977874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611327-A-G

121977882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611335-G-C

121977898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611350-A-T

121977974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611417-A-T

121977976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611419-A-G

121981662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611562-A-G

121981662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611562-A-T

121981700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611601-G-A

121981726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611627-G-A

121981833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611719-A-G

121982021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611887-A-G

121982062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52611928-C-G

121982222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52612277-A-G

121982594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52612601-G-A

121982594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52612601-G-T

121982745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52612730-G-A

121982745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52612730-G-T

121982931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52612886-G-A

121982931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52612886-G-T

http://identifiers.org/hco/5/GRCh38#121994481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52616599-C-A

121994481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616599-C-T

121994525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616637-A-G

121994553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616667-A-G

http://identifiers.org/hco/5/GRCh38#121994569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52616680-C-A

121994569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616680-C-T

121994582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616688-G-A

121994582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616688-G-C

122009918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616828-C-T

122009962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616870-C-G

122009992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616877-C-G

122009995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616880-A-T

122010046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52616926-G-A

http://identifiers.org/hco/5/GRCh38#122010142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52617026-A-C

122010230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52617127-G-A

122011074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52618628-G-C

122011110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52618665-T-G

122011153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52618708-A-G

122011170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52618720-G-C

122011215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52618781-C-T

122011582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52619174-C-T

122011761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52619259-A-G

122011872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52619329-A-G

122011879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52619336-A-T

122012020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52619452-G-T

122012162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52619594-T-C

122018409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52619790-A-G

122018542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52619897-G-T

122018616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52619946-T-C

122018811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52620191-A-G

122018830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52620209-G-A

122018862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52620238-C-T

122018979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52620339-G-A

122019126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52620458-A-G

122019190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52620518-A-T

http://identifiers.org/hco/5/GRCh38#122019198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52620526-C-A

122019198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52620526-C-G

122019198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52620526-C-T

122019239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52620563-A-G

122019262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 52620586-A-G

122019303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52620627-T-A

122019310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52620634-T-C

122019387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52620700-G-C

122019843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52621104-G-T

http://identifiers.org/hco/5/GRCh38#122019989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52621226-C-A

122019989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52621226-C-G

122019989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52621226-C-T

http://identifiers.org/hco/5/GRCh38#122019994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52621231-A-C

122019994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52621231-A-G

122019994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52621231-A-T

http://identifiers.org/hco/5/GRCh38#122020001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52621238-C-A

122020001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52621238-C-T

122020045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52621280-A-G

122020064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron variant
orthologous variants: 52621299-A-T

http://identifiers.org/hco/5/GRCh38#122020088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52621323-C-A

122020088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 52621323-C-G

122020104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52621339-T-C

122020131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52621366-A-G

122020137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621372-G-C

122020166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621401-A-G

http://identifiers.org/hco/5/GRCh38#122020169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52621404-C-A

122020169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621404-C-T

http://identifiers.org/hco/5/GRCh38#122020201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52621436-A-C

122020201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621436-A-G

122020214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621449-G-A

122020233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621471-T-A

122020233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52621471-T-C

http://identifiers.org/hco/5/GRCh38#122020247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52621485-A-C

122020247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621485-A-G

122020253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621491-C-T

122020266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52621504-G-A

122020266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52621504-G-C

http://identifiers.org/hco/5/GRCh38#122020274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52621512-C-A

122020274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621512-C-G

122020346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621584-C-T

122020371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52621609-T-A

122020371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52621609-T-C

122020371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: synonymous variant
orthologous variants: 52621609-T-G

122020384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621622-G-A

122020394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621632-A-G

122020427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621674-G-A

http://identifiers.org/hco/5/GRCh38#122020439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52621686-A-C

122020472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621713-A-G

122020502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense variant
orthologous variants: 52621743-A-G

122020542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52621783-T-C

122020560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52621801-G-A

122020580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52621821-G-T

122020596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52621837-T-C

122020628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52621869-G-A

http://identifiers.org/hco/5/GRCh38#122020644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52621885-A-C

122020644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52621885-A-G

122020715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52621956-G-A

122020726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52621967-A-G

122020755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 52621996-A-G

122020793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 52622034-G-A

122020827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622068-A-G

122020870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622109-T-C

122020883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622122-A-G

http://identifiers.org/hco/5/GRCh38#122020894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52622133-C-A

122020911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622154-T-C

http://identifiers.org/hco/5/GRCh38#122020912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52622155-C-A

122020912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622155-C-T

122020928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622171-G-A

122020928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622171-G-T

122020933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622176-C-T

122021030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622274-A-G

122021180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622338-A-G

122021267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622400-T-C

122021347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622471-T-G

122021473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622631-A-G

122021590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622720-A-G

122021605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622735-A-T

122022045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622816-G-T

122022246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622978-G-A

122022246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622978-G-T

122022253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622985-T-A

122022253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622985-T-C

http://identifiers.org/hco/5/GRCh38#122022267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52622998-A-C

122022267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622998-A-G

122022267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52622998-A-T

122022274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623006-C-G

122022274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623006-C-T

http://identifiers.org/hco/5/GRCh38#122022291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52623023-C-A

122022291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623023-C-T

122022460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623171-A-G

122022537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623248-A-G

122022549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623260-T-C

122022549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623260-T-G

122026760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623347-A-G

122026779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623364-A-G

122026786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623371-A-T

122026796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623381-G-A

122026796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623381-G-C

122026801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623386-A-G

http://identifiers.org/hco/5/GRCh38#122026827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52623412-C-A

http://identifiers.org/hco/5/GRCh38#122026897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52623475-C-A

122026897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623475-C-T

122026898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623476-T-A

122026898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52623476-T-C

122026961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 52623535-T-A

122027019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 52623593-C-T

http://identifiers.org/hco/5/GRCh38#122027133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52623705-C-A

122027133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52623705-C-T

122027351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52623766-A-G

122027351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52623766-A-T

122027409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52623825-T-C

122027442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52623858-T-C

http://identifiers.org/hco/5/GRCh38#122027456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52623872-C-A

122027482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52623889-A-G

122027727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52624297-A-G

http://identifiers.org/hco/5/GRCh38#122027932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52624462-A-C

122027932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52624462-A-G

122035485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628585-C-G

122035485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628585-C-T

122035686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628758-C-T

122035777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628851-C-T

122035793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52628869-A-G

122036147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52629191-C-T

122036170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52629214-A-G

122036170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52629214-A-T

122036353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52629427-G-A

122036353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52629427-G-T

122036363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52629437-A-G

122036411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52629485-T-C

122036620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52629678-C-T

122037210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630362-A-G

122037259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630409-G-A

122037646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630683-A-G

122037649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630686-C-G

122037669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630703-T-C

122037704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52630743-C-T

122038207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631129-G-A

http://identifiers.org/hco/5/GRCh38#122038307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52631208-A-C

http://identifiers.org/hco/5/GRCh38#122038387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52631278-C-A

122038396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631287-T-C

122038485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631425-G-T

122038546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631482-C-T

122038553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631489-C-T

122038622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631543-A-G

122038869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631776-C-G

122038869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631776-C-T

122039041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631972-A-G

122039063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52631993-T-A

122039080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632009-C-G

122039175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632099-T-C

122039187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632155-T-C

122039187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632155-T-G

122039210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632178-G-A

122039641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632628-G-A

122039760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632764-G-C

122039813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632803-T-C

122039815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52632805-T-C

122040160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52633602-T-G

122040190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52633632-G-A

122040585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634007-T-C

122040664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634106-A-T

122040960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634548-T-A

122040992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634603-A-G

http://identifiers.org/hco/5/GRCh38#122041020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52634629-A-C

122041022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634631-C-G

122041170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52634935-G-T

http://identifiers.org/hco/5/GRCh38#122041256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52635017-C-A

122041432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635176-T-C

122041435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635179-T-C

122041512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635286-A-G

122041523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635297-C-T

122041533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635307-T-C

122041582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635355-A-G

122041582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635355-A-T

122041723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635493-T-C

122041723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635493-T-G

122041777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635546-T-A

122041807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52635576-G-A

http://identifiers.org/hco/5/GRCh38#122042811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52638062-A-C

122042811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52638062-A-G

122043072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52638309-A-G

122043670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52638600-A-G

122043670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52638600-A-T

122043707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52638626-G-T

122057065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52639380-A-G

122057123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52639442-T-C

122057180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52639499-T-C

122057272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52639593-A-G

122057359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52639676-C-G

122057722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52639952-G-A

122057723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52639953-A-G

122058204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52641693-T-A

122058292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52641785-T-C

122058732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52642168-G-A

122058879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52642287-A-T

122059167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52642620-G-C

122059353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52642794-T-C

122059805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52643234-T-C

122059902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52643295-G-T

122059914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52643307-G-A

122059989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52643382-C-T

122060047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52643439-C-G

122060197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52643576-C-T

http://identifiers.org/hco/5/GRCh38#122060204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52643583-A-C

122060206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52643585-T-A

122060256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52643637-G-A

122060535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52643876-G-T

122061488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645248-A-T

122061609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645370-A-G

122061756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645514-A-T

122061771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645529-G-C

122061820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645568-T-C

122061996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645740-G-T

http://identifiers.org/hco/5/GRCh38#122062179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52645915-C-A

122062179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52645915-C-G

122063235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52649012-T-G

122063279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52649051-A-G

122063415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52649186-T-A

122063474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52649241-G-A

122063565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52649329-G-A

122063576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52649340-A-G

122063898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52649613-T-C

122063899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52649614-G-T

122064123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52649792-T-C

122064352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52649963-A-G

http://identifiers.org/hco/5/GRCh38#122064438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52650033-C-A

http://identifiers.org/hco/5/GRCh38#122064470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#52650054-C-A

122064470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52650054-C-T

http://identifiers.org/hco/5/GRCh38#122064560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52650157-C-A

122064593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650192-A-G

122064634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650231-G-A

122064796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650371-A-G

http://identifiers.org/hco/5/GRCh38#122064806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52650381-C-A

122064806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650381-C-T

122064829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650392-T-C

122064840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650403-A-G

122065078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650634-T-C

http://identifiers.org/hco/5/GRCh38#122065101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52650658-C-A

122065132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650690-G-T

122065166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650724-G-A

122065166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650724-G-T

122065236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650793-A-T

122065292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650846-G-A

http://identifiers.org/hco/5/GRCh38#122065316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52650870-C-A

122065329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52650883-G-T

http://identifiers.org/hco/5/GRCh38#122065554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52651116-C-A

122065627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52651193-G-A

122065854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52651450-A-T

122065888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52651484-A-G

122065892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52651492-C-T

122066056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52651635-T-C

122066286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52651854-A-G

122066326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52651896-T-C

http://identifiers.org/hco/5/GRCh38#122066378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52651944-C-A

122066378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52651944-C-G

122066450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652011-T-A

122066450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652011-T-C

http://identifiers.org/hco/5/GRCh38#122066478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52652039-C-A

122066478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652039-C-T

122066510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652069-T-A

http://identifiers.org/hco/5/GRCh38#122066558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52652114-A-C

122066558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652114-A-G

122066600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652156-A-T

122066689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652246-C-T

122066701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652259-C-T

122066777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652333-A-G

122066804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652360-A-G

122066805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652361-G-A

122066805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652361-G-T

http://identifiers.org/hco/5/GRCh38#122066829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52652385-A-C

122066829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652385-A-G

122066938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652491-T-G

122067151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52652740-T-C

122067586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52653131-T-C

http://identifiers.org/hco/5/GRCh38#122067793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52653305-C-A

122067793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52653305-C-T

122067994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52653489-G-A

122068164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52653648-T-A

122068164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52653648-T-G

http://identifiers.org/hco/5/GRCh38#122068170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52653654-C-A

122070147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52653960-G-C

http://identifiers.org/hco/5/GRCh38#122070255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52654098-C-A

122070255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654098-C-T

122070333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654177-G-T

122070379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654213-T-A

122070379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654213-T-C

122070379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654213-T-G

http://identifiers.org/hco/5/GRCh38#122070410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52654246-C-A

122070469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654291-A-G

122070503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 52654324-A-T

122070545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 52654366-G-A

122070545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654366-G-T

122070621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654442-A-G

122070646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654461-A-G

122070692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 52654507-A-G

122070693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 52654508-G-A

122070745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654560-T-C

http://identifiers.org/hco/5/GRCh38#122070785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52654577-A-C

http://identifiers.org/hco/5/GRCh38#122070805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52654597-A-C

122070842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654620-A-G

http://identifiers.org/hco/5/GRCh38#122071048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52654801-C-A

122071274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52654962-A-G

122071319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52655007-T-A

122071359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52655045-G-T

122071373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52655059-G-A

122071373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52655059-G-C

122071474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52655154-G-T

122071481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52655161-C-G

122071606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52655283-G-C

122071606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52655283-G-T

122071699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52655826-T-C

122072098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52656216-T-A

122072169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52656282-A-G

122072174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52656287-G-C

122072174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52656287-G-T

122072300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52656523-G-A

122072300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52656523-G-C

122072375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52656605-T-C

122072426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52656656-A-G

122072557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52656780-C-G

122072832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52657068-C-G

122072832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52657068-C-T

122073470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52657711-C-T

122073639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52657876-G-A

122073702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52657939-G-T

122073800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52658037-C-T

122073985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52658127-G-A

122074136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 52658278-A-G

122074223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52658365-T-A

http://identifiers.org/hco/5/GRCh38#122074251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52658389-C-A

122074258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52658396-A-G

http://identifiers.org/hco/5/GRCh38#122074268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52658417-C-A

122074462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659099-A-T

122074585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659225-T-A

122074585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659225-T-C

122074631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659271-C-T

122074796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659438-A-G

122074797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659439-T-C

122074913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659562-C-T

122074957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659606-G-C

122074957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659606-G-T

122074963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659612-T-A

122075200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659813-G-A

122075200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659813-G-T

122075242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659847-G-T

122075244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659849-A-G

122075244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659849-A-T

122075257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52659854-T-C

122075457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 52660026-T-G

122075694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52660248-T-G

122076371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 52660855-T-G

122076699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 52661188-A-G

122076937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 52661395-G-A

122077062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 52661492-C-G

122077370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 52661804-C-T

http://identifiers.org/hco/5/GRCh38#122077541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#52661975-C-A

122077682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26333
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 52662116-C-T