116496502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33979122-T-A

116496502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33979122-T-G

116496590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 33979044-T-A

http://identifiers.org/hco/6/GRCh38#116496615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33979017-C-A

116496615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 33979017-C-G

116496615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 33979017-C-T

116496662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 33978968-G-C

116496662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 33978968-G-T

116496681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 33978949-G-A

http://identifiers.org/hco/6/GRCh38#116496767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33978875-A-C

116496767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 33978875-A-G

116497112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33978583-T-A

116497112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33978583-T-C

http://identifiers.org/hco/6/GRCh38#116497125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33978571-A-C

116497144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33978549-T-C

116497150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33978543-G-A

116497150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33978543-G-T

116497197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33978511-T-A

116497197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33978511-T-C

http://identifiers.org/hco/6/GRCh38#116497218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33978490-A-C

116497218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33978490-A-G

116497405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33978291-C-T

116497511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33978187-T-C

116497889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33977814-T-A

116498280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33977421-C-T

116498542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33977162-A-G

116498569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33977055-C-T

116498613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33977013-A-G

116498673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33976954-T-G

116498747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33976916-T-C

116498892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33976728-C-T

116498930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33976687-G-A

116499380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33976275-A-T

116499383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33976272-T-C

116499386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33976269-T-G

http://identifiers.org/hco/6/GRCh38#116499674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33976061-C-A

116499722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33976017-T-C

116499794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33975933-C-T

116500193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33975492-G-A

http://identifiers.org/hco/6/GRCh38#116500464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33975004-C-A

http://identifiers.org/hco/6/GRCh38#116500571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33974853-C-A

116500571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: synonymous variant
orthologous variants: 33974853-C-G

116500696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33974730-C-T

116500724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33974705-G-A

116500724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33974705-G-T

116500763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33974680-G-A

116500763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33974680-G-T

116500797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33974642-G-A

116500797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33974642-G-T

116507323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33974127-G-A

116507323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33974127-G-T

http://identifiers.org/hco/6/GRCh38#116507919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33973649-A-C

116508160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33973415-C-T

116508203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33973375-T-C

116508253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33973328-G-A

116508265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33973316-A-G

116508431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33973150-C-T

116508451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33973136-A-G

116511306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33972832-G-A

116511306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33972832-G-T

116511578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron_variant, undefined
orthologous variants: 33972566-T-C

116511652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33972499-T-A

116511652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33972499-T-C

116511652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33972499-T-G

116511952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron_variant, missense_variant
orthologous variants: 33972176-A-G

116512352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33971789-A-G

116512352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33971789-A-T

116512928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33971207-G-T

116512931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33971203-C-T

116512993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33971141-T-C

116513002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33971132-C-T

116513170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970977-C-T

http://identifiers.org/hco/6/GRCh38#116513467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33970687-A-C

116513522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970635-A-G

116513640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970528-T-A

116513640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970528-T-C

116513675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970493-G-A

116513820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970349-A-G

116513954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970237-T-C

116513963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970228-T-C

116513977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970214-G-C

116514111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970104-G-T

116514116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970099-G-A

116514194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33970020-C-T

http://identifiers.org/hco/6/GRCh38#116514678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33969606-C-A

116514895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33969215-T-C

116514936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33969174-T-C

116514967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33969146-C-G

116515061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33969054-A-G

116515061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33969054-A-T

116515121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33968969-G-A

116515282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33968775-A-G

116515457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33968633-T-G

116515474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33968617-G-A

116515474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33968617-G-T

116515481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33968610-T-A

116515523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33968570-T-A

116515538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33968555-T-C

116515648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron_variant, missense_variant
orthologous variants: 33968461-A-G

116515936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron_variant, missense_variant
orthologous variants: 33968173-C-T

116516034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33968076-T-G

http://identifiers.org/hco/6/GRCh38#116516088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33968021-C-A

116516088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33968021-C-T

116516093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33968016-G-T

116516115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967997-A-G

116516145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967966-G-A

116516145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967966-G-T

http://identifiers.org/hco/6/GRCh38#116516151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33967960-C-A

116516151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967960-C-T

116516396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967753-G-A

116516396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967753-G-T

http://identifiers.org/hco/6/GRCh38#116516449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33967699-A-C

116516489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967654-C-T

116516616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967531-T-A

116516848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967354-T-C

116516901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967301-G-A

116516901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967301-G-C

116516901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967301-G-T

http://identifiers.org/hco/6/GRCh38#116518163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33966253-C-A

116518346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966441-A-G

116518474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966531-A-G

116518496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966554-A-G

116518531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966580-A-G

http://identifiers.org/hco/6/GRCh38#116518578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33966630-C-A

116518609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966649-G-C

116518609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966649-G-T

116518629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966662-G-A

116518629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966662-G-T

116518641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966674-T-C

116518659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966692-A-G

116518665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966698-T-A

116518697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966727-G-T

http://identifiers.org/hco/6/GRCh38#116518703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33966733-C-A

116518712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966742-G-T

116518739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966769-G-A

http://identifiers.org/hco/6/GRCh38#116518816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33966846-C-A

116518890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966902-G-A

116518890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33966902-G-T

116519036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967056-T-A

116519036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967056-T-C

http://identifiers.org/hco/6/GRCh38#116519056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33967076-C-A

116519072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967090-T-C

116519077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967095-G-A

116519077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967095-G-T

116519093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967111-G-A

116519093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967111-G-T

116519095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967113-A-G

http://identifiers.org/hco/6/GRCh38#116519163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33967177-C-A

116519170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33967184-G-T

116528464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33965409-A-T

116528603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33965273-A-G

116528619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33965257-G-T

116528937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33964944-C-G

http://identifiers.org/hco/6/GRCh38#116529039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33964849-C-A

116529126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33964762-G-T

116529145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33964743-T-C

116529184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33964700-G-A

116529186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33964698-G-T

116529206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33964678-G-A

116529206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33964678-G-C

http://identifiers.org/hco/6/GRCh38#116529297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33964602-C-A

116529297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33964602-C-T

116529317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33964582-A-G

116529523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33964453-A-G

116529535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33964446-T-A

116529538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33964443-G-C

116529974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33963521-G-A

116530136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33963395-A-G

116530468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962991-G-A

116530484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962975-T-C

116530544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962920-A-T

http://identifiers.org/hco/6/GRCh38#116530681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33962777-C-A

116530947-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962582-T-A

116530947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962582-T-G

http://identifiers.org/hco/6/GRCh38#116530949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33962580-C-A

116530949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962580-C-G

116530949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962580-C-T

116530987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962553-T-A

116531112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962431-G-A

116531112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962431-G-C

116531265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33962283-A-G

116531476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33961864-G-A

116531554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33961805-G-A

116531641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33961728-T-C

116531745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33961623-C-T

116531815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33961553-T-C

116532004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33961459-G-A

http://identifiers.org/hco/6/GRCh38#116532012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33961451-C-A

116532012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33961451-C-T

116532034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33961429-T-C

116532847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33959913-A-G

116533006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33959767-G-C

116533071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33959711-G-A

116533084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33959697-T-C

http://identifiers.org/hco/6/GRCh38#116533089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33959692-C-A

http://identifiers.org/hco/6/GRCh38#116533334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33959476-A-C

116533605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron_variant, undefined
orthologous variants: 33959220-T-G

116533613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33959212-G-A

116533667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron_variant, undefined
orthologous variants: 33959164-A-G

116533846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33959023-C-G

116534107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33958376-C-T

116534108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33958375-G-T

116534120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33958368-C-T

116534188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33958302-T-C

116534210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33958280-T-C

http://identifiers.org/hco/6/GRCh38#116534262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33958217-A-C

116534407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33957976-G-A

116534413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33957970-T-C

http://identifiers.org/hco/6/GRCh38#116534467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33957917-A-C

116534467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33957917-A-T

116534626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33957756-G-C

116534633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33957542-T-C

116534738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33957431-A-G

116534779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33957390-A-G

116534870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33957304-G-A

http://identifiers.org/hco/6/GRCh38#116535133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33951667-A-C

116535443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33951166-C-T

http://identifiers.org/hco/6/GRCh38#116535561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33951051-A-C

116535670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33950934-T-C

116535683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33950921-T-C

116535774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33950113-T-A

116535877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33949965-A-G

http://identifiers.org/hco/6/GRCh38#116535916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33949929-A-C

116535948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33949903-A-T

116536437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33947754-T-C

116536588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33947608-T-C

116536667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33947552-G-A

116536669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33947550-G-A

116536765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33947458-A-T

116536930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33947299-C-T

116537039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33947189-A-G

116537115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33947116-G-A

116537182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33947059-G-A

116538347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33944772-A-G

116538503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33944641-C-G

116538697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33944430-T-G

116539264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33943753-T-A

116539455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33943528-T-C

116539799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33943179-A-G

116540284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33941470-A-G

116540284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33941470-A-T

116540285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33941469-T-C

116540367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron_variant, missense_variant
orthologous variants: 33941234-G-A

116540451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron_variant, missense_variant
orthologous variants: 33941150-A-G

116540451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron_variant, missense_variant
orthologous variants: 33941150-A-T

116540497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33941111-C-G

116540597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33941070-G-T

116540637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33941030-A-G

http://identifiers.org/hco/6/GRCh38#116540653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33941014-C-A

116540679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33940990-T-G

116540907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33940806-G-A

116541604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33939795-A-T

116541880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33939561-A-G

116541932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33939510-T-C

http://identifiers.org/hco/6/GRCh38#116542050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33939395-A-C

116542078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33939367-T-A

116542121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33939320-G-T

116542166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33939279-G-A

116542192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33939253-G-A

116542215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33939230-A-G

http://identifiers.org/hco/6/GRCh38#116542332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33939127-A-C

116542332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33939127-A-T

116542539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33938913-C-T

116542755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33936638-A-T

116542808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33936587-A-G

116543091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33936292-C-G

116543268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33936136-C-G

116543268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33936136-C-T

116543273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33936131-A-G

116543274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33936130-T-C

116543353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 33936053-C-T

116543489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33935919-A-G

http://identifiers.org/hco/6/GRCh38#116543522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33935886-C-A

116543522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33935886-C-T

116543621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33935812-A-G

116543633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33935800-T-G

116543689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33935740-A-G

116543689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33935740-A-T

116543716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33935715-C-G

http://identifiers.org/hco/6/GRCh38#116543754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33935675-C-A

116543754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33935675-C-T

116543869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 33935565-A-G

116544076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33934311-C-T

116544432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33933928-T-C

116544674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33933671-A-G

116544718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33933627-C-G

http://identifiers.org/hco/6/GRCh38#116544741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33933604-C-A

116544788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33933555-C-T

http://identifiers.org/hco/6/GRCh38#116544997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33933334-A-C

116545059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33933252-A-G

116545280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33933082-A-T

116545330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33933028-G-A

116545330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33933028-G-T

116545336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33933022-T-A

116545336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33933022-T-C

http://identifiers.org/hco/6/GRCh38#116545370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33933000-C-A

116545383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33932983-T-A

116545421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: intron variant
orthologous variants: 33932944-A-G

116545598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33932770-T-A

116545638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33932730-G-A

116545638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21090
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 33932730-G-T