45631466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122605224-G-T

http://identifiers.org/hco/15/GRCh38#45631481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122605238-C-A

45631481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122605238-C-T

45631547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122605298-G-T

45631567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122605318-G-T

45631589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 122605356-T-G

45631615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 122605378-C-T

http://identifiers.org/hco/15/GRCh38#45631664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122605413-C-A

45631674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 122605423-T-C

http://identifiers.org/hco/15/GRCh38#45631697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#122605445-C-A

45631697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 122605445-C-T

45631717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 122605464-G-A

45631717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 122605464-G-T

http://identifiers.org/hco/15/GRCh38#45631842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122605623-C-A

45631842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 122605623-C-T

http://identifiers.org/hco/15/GRCh38#45631854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122605635-C-A

45631854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 122605635-C-T

45632015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 122605781-A-G

45632582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122606145-G-A

45632608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122606168-C-T

http://identifiers.org/hco/15/GRCh38#45632684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122606226-A-C

45632747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122606289-C-T

http://identifiers.org/hco/15/GRCh38#45632824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122606350-C-A

45634275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122606817-G-C

45634275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122606817-G-T

45634346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122606868-C-T

http://identifiers.org/hco/15/GRCh38#45634436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122606946-C-A

45634436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122606946-C-T

45634437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122606947-T-C

45634634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122607090-G-A

45634634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122607090-G-T

45634662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122607111-C-G

45634726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 122607116-C-T

http://identifiers.org/hco/15/GRCh38#45634762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#122607135-C-A

45634893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 122607189-T-C

45634896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 122607192-T-A

45635001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122607262-C-T

http://identifiers.org/hco/15/GRCh38#45635044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122607305-A-C

45635193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122607403-G-T

45635203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122607415-C-T

45635235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122607438-G-A

45635235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122607438-G-C

45635438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122607624-C-T

45635484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122607652-C-G

45635484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122607652-C-T

45635775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122607906-G-A

45637356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122608684-G-C

45637356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122608684-G-T

45637370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122608698-G-T

45637392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122608720-A-G

45637395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122608723-T-C

45637831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122609096-C-G

http://identifiers.org/hco/15/GRCh38#45637873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122609149-C-A

45637875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122609151-C-T

45639799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122609389-G-A

45639802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122609395-G-A

45639924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122609524-C-T

45640217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122609855-T-C

45640336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122609971-C-T

http://identifiers.org/hco/15/GRCh38#45640344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122609979-C-A

45640463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122610090-C-T

http://identifiers.org/hco/15/GRCh38#45640469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122610096-A-C

45640894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122611666-G-A

45641203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122611944-C-T

http://identifiers.org/hco/15/GRCh38#45641499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#122613004-A-C

45641852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122613335-G-A

45642073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122613515-C-G

45642365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122613782-C-T

45642421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, undefined
orthologous variants: 122613841-T-C

45642497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122613910-C-T

45643498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122617626-A-T

45643499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122617627-A-G

http://identifiers.org/hco/15/GRCh38#45644028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122618135-C-A

45644736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122618509-G-C

http://identifiers.org/hco/15/GRCh38#45645319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122619045-C-A

45645347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122619068-G-A

45645584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122619226-C-T

45645594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122619236-T-C

45645601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122619243-G-C

45645604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122619245-C-G

45645604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122619245-C-T

45645648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122619285-T-C

45645732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122619379-T-C

45646337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122621157-C-G

45649037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122621930-C-T

45653008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122622606-T-G

45653068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122622658-G-A

45653226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122622807-A-G

45653288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122622858-C-T

45653368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122622934-T-C

45653476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122623019-T-C

45653519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122623063-C-T

45653550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122623094-G-A

45654458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122623663-T-C

45654496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122623701-G-A

45655212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122623805-G-A

http://identifiers.org/hco/15/GRCh38#45657285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122625082-A-C

45657285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122625082-A-T

45657315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122625111-A-G

http://identifiers.org/hco/15/GRCh38#45657332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122625128-C-A

45657642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122625385-C-T

45657673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122625412-T-C

45658193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122625858-C-T

45658201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122625866-T-C

http://identifiers.org/hco/15/GRCh38#45658208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122625873-C-A

45658358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626015-C-G

45658358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626015-C-T

45658431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626090-G-T

45658559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626211-C-G

45658563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626215-A-G

45658658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626538-A-G

45658688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626661-G-A

45658728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626705-C-G

45658728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626705-C-T

http://identifiers.org/hco/15/GRCh38#45658765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122626735-A-C

45658765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626735-A-T

http://identifiers.org/hco/15/GRCh38#45658780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122626750-C-A

45658780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626750-C-G

45658792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122626766-T-C

45658939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: missense variant
orthologous variants: 122626896-G-A

45658939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: missense variant
orthologous variants: 122626896-G-T

http://identifiers.org/hco/15/GRCh38#45658964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122626921-A-C

45658964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: missense variant
orthologous variants: 122626921-A-G

45658964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: missense variant
orthologous variants: 122626921-A-T

45658980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: 122626937-G-A

45658980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: 122626937-G-C

45658980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: 122626937-G-T

45659004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: 122626961-C-G

45659004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: 122626961-C-T

http://identifiers.org/hco/15/GRCh38#45659085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122627042-C-A

45659085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: 122627042-C-T

45659183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122627130-G-T

45659206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122627153-G-A

45659206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122627153-G-T

45659332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122627247-T-C

45659355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122627342-C-T

45659655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122627637-T-C

45660550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122628219-C-T

45660635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122628322-G-A

45660713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122628399-G-C

45660855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122628533-C-T

45661343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122628755-A-G

http://identifiers.org/hco/15/GRCh38#45661352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122628764-A-C

45661369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122628772-G-C

45661458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122628836-C-G

45661806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122629228-T-C

http://identifiers.org/hco/15/GRCh38#45661837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122629260-A-C

45661837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122629260-A-G

45661837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122629260-A-T

45661878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122629299-C-G

45661885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122629308-A-G

45661885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122629308-A-T

45662138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122629561-G-A

45662157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122629580-A-G

http://identifiers.org/hco/15/GRCh38#45662454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122629836-C-A

45664559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122633119-G-A

45664704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122632980-G-C

45664759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122632936-A-T

45664760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122632935-G-A

45665325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122632397-A-G

45665397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122632330-G-A

45665643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122632151-G-A

45665847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122632119-G-A

45666716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122631422-C-T

45667650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122631023-G-T

45667652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122631021-A-G

45668325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122633319-C-T

45668437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122633419-C-T

45668449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122633431-A-G

45668478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122633475-G-A

45668836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122633790-G-A

45669002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122633938-A-G

45669664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122634127-G-A

45669720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122634182-C-T

45670019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122634361-T-G

45670061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122634397-T-C

45670093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122634448-T-C

45670349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122634703-T-C

45670425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122634772-C-T

45670426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122634773-G-A

45670679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122635020-C-T

45670756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122635104-G-C

45671126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122636873-A-G

45671476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122637139-C-G

http://identifiers.org/hco/15/GRCh38#45671512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122637174-C-A

45671576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122637240-G-A

45671790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122637551-G-A

45671806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122637567-G-A

45671806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122637567-G-T

45671842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122637607-T-C

45673120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122638939-C-G

45673243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122639056-A-G

45673275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122639090-T-C

45673396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122639215-G-A

45673484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122639300-T-G

45673530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122639345-G-T

45673573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122639393-T-C

45673573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122639393-T-G

45673586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122639937-T-C

http://identifiers.org/hco/15/GRCh38#45673618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122639969-A-C

45673618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: 122639969-A-G

http://identifiers.org/hco/15/GRCh38#45673756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122640107-A-C

45673819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 122640169-G-C

45673820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, missense_variant
orthologous variants: 122640170-G-A

45673820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron_variant, missense_variant
orthologous variants: 122640170-G-T

45673856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122640203-G-T

45673995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122640323-T-C

45674534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122641043-A-G

45674808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122641312-C-T

45674923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122641427-G-A

http://identifiers.org/hco/15/GRCh38#45676208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122641789-C-A

45676208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: 122641789-C-T

http://identifiers.org/hco/15/GRCh38#45676362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122641942-C-A

45676362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122641942-C-T

http://identifiers.org/hco/15/GRCh38#45676371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122641951-C-A

45676449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122642006-T-C

http://identifiers.org/hco/15/GRCh38#45677298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122643052-C-A

45677603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122643297-C-T

45678360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122643648-T-C

45678442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122643731-C-T

45678575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122643869-A-T

45678606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122643894-A-T

45678634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122643914-G-T

45678665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122643945-T-C

45678983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122644190-G-A

45678983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122644190-G-T

45679001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122644208-T-G

45679143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122644363-G-T

45679346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122644574-G-C

45679383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122644614-T-A

45681460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122644864-C-G

45681460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122644864-C-T

http://identifiers.org/hco/15/GRCh38#45681652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122645036-A-C

45681728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122645102-C-T

http://identifiers.org/hco/15/GRCh38#45681743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122645117-C-A

45681981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122645346-G-C

45682364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122645722-T-A

45682364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122645722-T-G

45682427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122645791-G-T

45682600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: 122645964-A-T

45683251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122646353-C-G

http://identifiers.org/hco/15/GRCh38#45683435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122646538-C-A

45683577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122646687-G-A

45683738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122646794-A-G

45684639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122647277-C-T

45684928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122647549-C-T

45684986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122647607-G-A

45685300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122647796-G-A

45685344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122647836-G-A

45685374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122647858-G-A

45685433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122647916-T-G

45685530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122647946-G-A

45685530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122647946-G-C

45685530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122647946-G-T

45685635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122648048-C-G

45685635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122648048-C-T

http://identifiers.org/hco/15/GRCh38#45685660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122648073-C-A

45685748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122648152-C-G

45685748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122648152-C-T

45685751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122648155-T-C

http://identifiers.org/hco/15/GRCh38#45688214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122649376-C-A

45688214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122649376-C-T

45688257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122649425-A-T

45688325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122649481-T-C

45688436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122649591-A-G

45688453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122649608-T-A

45688453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122649608-T-C

http://identifiers.org/hco/15/GRCh38#45688490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122649625-C-A

45688490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122649625-C-G

45688490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122649625-C-T

45688893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122649677-A-T

http://identifiers.org/hco/15/GRCh38#45688955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122649750-C-A

45688955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122649750-C-T

45689200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: synonymous variant
orthologous variants: 122650035-T-C

45689251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122650101-G-A

http://identifiers.org/hco/15/GRCh38#45689342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122650333-C-A

45689342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122650333-C-T

45689410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122650432-T-A

45689410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122650432-T-C

45689410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 122650432-T-G

45690416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122650705-A-G

45690469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122650760-C-G

45690469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122650760-C-T

45690644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122650903-A-G

45690644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122650903-A-T

http://identifiers.org/hco/15/GRCh38#45690851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122651102-C-A

45690851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122651102-C-T

45690933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: intron variant
orthologous variants: 122651163-C-G

http://identifiers.org/hco/15/GRCh38#45691070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122651298-C-A

http://identifiers.org/hco/15/GRCh38#45691071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122651299-C-A

45691071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3 prime UTR variant
orthologous variants: 122651299-C-T

http://identifiers.org/hco/15/GRCh38#45691143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122651363-A-C

45691143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3 prime UTR variant
orthologous variants: 122651363-A-G

45691143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3 prime UTR variant
orthologous variants: 122651363-A-T

http://identifiers.org/hco/15/GRCh38#45691207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122651415-C-A

45691207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3 prime UTR variant
orthologous variants: 122651415-C-T

http://identifiers.org/hco/15/GRCh38#45691276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20390
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122651480-C-A