http://identifiers.org/hco/10/GRCh38#125836511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133322837-A-C

125836511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133322837-A-G

125836672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 133322944-G-T

125836841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 133323111-A-T

125836926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133323188-G-A

125836926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133323188-G-T

125836944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133323206-G-T

125836955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133323214-T-C

125837005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133323262-G-A

125837005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133323262-G-T

125837287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133323450-G-A

125837396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133323522-C-G

125837852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133323666-C-T

125837867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133323699-A-G

125838136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133323813-A-G

125838137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133323814-A-G

125838194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133323866-C-T

125838304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 133323976-G-A

125838394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 133324066-G-A

125838398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324070-G-A

125838398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324070-G-T

125838415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324085-G-A

125838415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324085-G-C

125838415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324085-G-T

125838459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324110-A-G

http://identifiers.org/hco/10/GRCh38#125838469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133324120-C-A

125838470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324121-A-G

http://identifiers.org/hco/10/GRCh38#125838529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133324177-C-A

125838532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324181-G-A

125838532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324181-G-T

125838631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324259-G-A

125838648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324276-C-T

125838691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324318-C-T

125838869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324639-A-G

125838877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324647-T-A

http://identifiers.org/hco/10/GRCh38#125838912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133324689-A-C

http://identifiers.org/hco/10/GRCh38#125838971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133324742-C-A

125838985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133324756-C-T

125839042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, missense_variant
orthologous variants: 133324812-G-C

125839127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 133324897-A-G

125839127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, missense_variant
orthologous variants: 133324897-A-T

125839163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 133324933-A-G

125839309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133325026-A-G

125839325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133325042-G-T

125839726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133325364-G-A

125839726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133325364-G-C

125840063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133325674-C-T

125840118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133325731-T-G

125840419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133325825-C-T

125840560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133325864-G-A

125840781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133326059-A-G

125840787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133326065-T-C

125840787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133326065-T-G

125840804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133326083-A-G

125840809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133326088-A-G

125840815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133326093-A-G

125840816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133326094-A-G

http://identifiers.org/hco/10/GRCh38#125840837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133326115-A-C

125840837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133326115-A-G

125841078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133326354-A-G

125841087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133326363-G-T

125841215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133326493-T-C

125841250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 133326518-G-A

125841260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 133326528-G-A

125841321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, stop_gained
orthologous variants: 133326589-C-T

http://identifiers.org/hco/10/GRCh38#125841363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133326630-A-C

125841415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326681-A-G

125841419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326685-C-T

125841421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326687-T-A

125841431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326697-A-G

125841442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326708-T-C

125841444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326710-G-A

125841445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326711-T-A

125841445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326711-T-G

http://identifiers.org/hco/10/GRCh38#125841466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133326739-A-C

125841468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326741-T-C

http://identifiers.org/hco/10/GRCh38#125841490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133326766-C-A

125841490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326766-C-T

125841512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326785-A-T

125841555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133326809-T-A

125841973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133327155-T-C

http://identifiers.org/hco/10/GRCh38#125842006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133327185-C-A

125842006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133327185-C-T

125845941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133329100-C-G

125845992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133329150-C-G

125845992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133329150-C-T

125846108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133329259-G-A

http://identifiers.org/hco/10/GRCh38#125846250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133329752-C-A

http://identifiers.org/hco/10/GRCh38#125848694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133330513-C-A

125850824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133332178-C-G

125850824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133332178-C-T

125851109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133332491-C-T

125851221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133332683-G-T

125851384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133332842-T-C

125852312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 133335716-A-G

125852330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 133335734-A-G

125852741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133336124-G-A

125852741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133336124-G-T

125852927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133336257-T-C

125853003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133336344-A-T

125853099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133336438-G-T

http://identifiers.org/hco/10/GRCh38#125853107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133336446-C-A

125853107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133336446-C-T

125853473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133338302-A-G

http://identifiers.org/hco/10/GRCh38#125853518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133338339-C-A

125853518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133338339-C-T

125853561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133338368-T-C

125853626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133338418-A-T

http://identifiers.org/hco/10/GRCh38#125853690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133338714-C-A

125853690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133338714-C-T

125853708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133338729-T-C

http://identifiers.org/hco/10/GRCh38#125853778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133338782-C-A

125853801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133338810-A-G

125853801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133338810-A-T

125854084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 133339041-A-G

125854271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133339229-A-G

125854297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133339255-A-G

125854321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133339272-T-A

125854321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133339272-T-C

125854321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133339272-T-G

125854364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133339307-G-A

125854364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133339307-G-T

125856282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133342261-C-T

125856286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133342265-A-G

http://identifiers.org/hco/10/GRCh38#125856482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133342433-A-C

125856597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133342548-G-A

125857099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133342700-A-T

http://identifiers.org/hco/10/GRCh38#125857400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133342876-C-A

125857400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133342876-C-T

125857401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133342877-G-A

125857453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133342931-C-G

125857460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133342938-G-T

125859588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133344142-G-A

125859588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133344142-G-C

http://identifiers.org/hco/10/GRCh38#125859592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133344146-C-A

125859592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133344146-C-T

125859649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: missense variant
orthologous variants: 133344204-T-G

125859888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: synonymous variant
orthologous variants: 133344443-A-G

125859949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: missense variant
orthologous variants: 133344504-C-T

http://identifiers.org/hco/10/GRCh38#125860030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133344584-A-C

125860030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133344584-A-G

125860030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133344584-A-T

125860049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133344595-G-T

125860051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133344597-C-T

125860086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133344624-A-G

125860382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133344976-T-C

125860382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133344976-T-G

125860445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133345018-C-T

125860600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133345188-G-T

125860601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133345189-T-A

125860709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133345365-A-T

125860729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133345385-T-C

125861730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133345551-A-G

125861887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133345715-T-G

125861891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133345719-G-A

125861992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133345812-G-A

125862333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133346272-T-C

125862426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133346372-T-C

125862470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133346434-A-T

125862565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133346568-A-T

125862574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133346577-G-C

125862725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133346689-T-C

125863081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133346989-A-G

125863185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133347160-G-C

125863238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133347228-A-G

125863583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133347683-G-T

125863794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133347993-T-A

125863898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133348107-T-C

125864128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133348320-A-G

http://identifiers.org/hco/10/GRCh38#125866041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133349422-C-A

125866075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133349456-C-T

125866183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133349569-G-A

125866188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133349574-T-C

125866202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133349588-C-T

125866297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133349690-A-T

125866423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133349865-G-A

125866696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133350275-G-T

125866919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133350489-T-A

125866919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133350489-T-C

125866976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133350558-C-G

125866976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133350558-C-T

http://identifiers.org/hco/10/GRCh38#125866980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133350562-A-C

http://identifiers.org/hco/10/GRCh38#125867100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133350682-A-C

125867100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: synonymous variant
orthologous variants: 133350682-A-G

125867130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: synonymous variant
orthologous variants: 133350712-G-A

125867130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: synonymous variant
orthologous variants: 133350712-G-C

125867547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133351067-T-A

125867547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133351067-T-C

125867974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133351449-T-C

125867993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133351467-C-T

125873089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133353717-T-C

125873401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133353968-C-T

125873437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133353991-C-G

125873437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133353991-C-T

125873541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133354070-A-G

http://identifiers.org/hco/10/GRCh38#125873735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133354206-A-C

125873996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133356095-C-T

125874043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133356131-C-T

125874099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133356183-T-G

125877262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133359630-T-C

125877269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133359637-G-A

125877269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133359637-G-C

125877333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133359682-G-A

125878048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133359917-G-C

125878149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133360015-C-T

125880528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133361114-G-T

http://identifiers.org/hco/10/GRCh38#125880636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133361222-A-C

125880746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: missense variant
orthologous variants: 133361332-C-T

125880864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5 prime UTR variant
orthologous variants: 133361450-G-A

125881071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 133361642-A-G

125881100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133361670-G-A

125881100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133361670-G-T

http://identifiers.org/hco/10/GRCh38#125881277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133361814-C-A

125881535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133362057-A-G

125882409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133362845-A-G

125882411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133362847-T-C

125882989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133363308-T-C

125883991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133364705-T-C

125884188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133364885-G-A

125884357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133365262-A-G

125886540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133367124-A-G

125886758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133367297-C-T

125886995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133367476-G-C

125887088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133367546-G-C

125887536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133368003-T-G

125888640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133368814-T-C

125888662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133368838-A-T

http://identifiers.org/hco/10/GRCh38#125889412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133370602-A-C

125889491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133370691-T-C

125889494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133370694-T-A

125889513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133370713-C-T

125889538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133370738-C-T

125889664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133370774-C-T

125889788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133370894-C-G

125889788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133370894-C-T

125889991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133371091-C-T

http://identifiers.org/hco/10/GRCh38#125890067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133371265-C-A

125890435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133372103-G-T

125891190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373283-C-G

125891252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373322-T-A

125891359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373416-T-C

125891364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373421-T-A

125891379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373580-G-A

125891522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373650-A-G

125891722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373787-T-C

125891725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373790-A-T

125891746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373811-T-C

http://identifiers.org/hco/10/GRCh38#125891788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133373844-C-A

125891788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373844-C-T

125891822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373879-T-C

125891823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373880-T-A

http://identifiers.org/hco/10/GRCh38#125891846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133373897-A-C

125891846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373897-A-T

125891895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373934-C-G

125891895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373934-C-T

125891928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373968-G-A

125891942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133373984-T-C

http://identifiers.org/hco/10/GRCh38#125892090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133374111-A-C

125892142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133374172-C-G

125892142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133374172-C-T

http://identifiers.org/hco/10/GRCh38#125892151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133374181-C-A

125892151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133374181-C-G

125892205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133374240-A-G

125892215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133374250-G-A

http://identifiers.org/hco/10/GRCh38#125892216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133374251-C-A

125892376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133374445-C-T

http://identifiers.org/hco/10/GRCh38#125892399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133374467-C-A

125892399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133374467-C-G

http://identifiers.org/hco/10/GRCh38#125892404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133374472-C-A

125892404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133374472-C-T

http://identifiers.org/hco/10/GRCh38#125892978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133375388-A-C

125892978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133375388-A-G

125893001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133375423-C-T

http://identifiers.org/hco/10/GRCh38#125893010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133375434-C-A

125893010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133375434-C-T

http://identifiers.org/hco/10/GRCh38#125893170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133375569-C-A

125893850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133375873-T-C

125893852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133375875-T-C

125893954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133375975-T-C

125894006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376029-A-G

125894007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376030-T-C

125894064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376064-T-C

http://identifiers.org/hco/10/GRCh38#125894083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133376083-C-A

125894103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376118-T-C

125894103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376118-T-G

125894109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376124-G-A

http://identifiers.org/hco/10/GRCh38#125894307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133376261-C-A

125894433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376347-T-C

125894703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376593-A-G

125894760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376656-G-A

125894760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376656-G-T

http://identifiers.org/hco/10/GRCh38#125894836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133376725-C-A

125894836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376725-C-T

125894892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376775-A-G

125894938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376806-T-A

125894938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133376806-T-G

125895240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133377051-T-C

http://identifiers.org/hco/10/GRCh38#125895433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133377241-C-A

http://identifiers.org/hco/10/GRCh38#125895440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133377248-A-C

125895663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133377487-C-G

125895672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133377496-G-A

125895683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133377507-T-G

http://identifiers.org/hco/10/GRCh38#125895742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133377561-A-C

125895902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133377716-A-G

125895902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133377716-A-T

125895942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133377870-C-T

125895990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133377941-G-A

125895990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133377941-G-T

125896019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133377995-A-G

http://identifiers.org/hco/10/GRCh38#125896084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133378112-C-A

125896084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133378112-C-G

125896084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133378112-C-T

125896107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133378137-G-A

125896107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron variant
orthologous variants: 133378137-G-T

http://identifiers.org/hco/10/GRCh38#125896116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133378158-A-C

125896116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133378158-A-G

125896116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: 133378158-A-T

http://identifiers.org/hco/10/GRCh38#125896191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133378306-C-A

http://identifiers.org/hco/10/GRCh38#125896327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133378422-C-A

125896327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5 prime UTR variant
orthologous variants: 133378422-C-G

125896327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5 prime UTR variant
orthologous variants: 133378422-C-T

125896328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5 prime UTR variant
orthologous variants: 133378423-G-A

125896328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5 prime UTR variant
orthologous variants: 133378423-G-T

125896449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16717
most severe consequence: 5 prime UTR variant
orthologous variants: 133378487-C-G