56955113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 33946926-A-G

56955121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33946922-G-A

56955121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33946922-G-T

56955126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33946917-G-A

56955126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33946917-G-T

56955130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33946913-G-T

http://identifiers.org/hco/6/GRCh38#56955165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#33946894-C-A

56955165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 33946894-C-T

http://identifiers.org/hco/6/GRCh38#56955210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33946846-C-A

56955210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33946846-C-T

56955273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 33946788-G-A

56955283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 33946778-A-G

http://identifiers.org/hco/6/GRCh38#56955304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#33946757-C-A

56955349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 33946714-A-G

56955508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: 33946590-C-T

56955837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: 33946319-G-A

56955837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: 33946319-G-C

http://identifiers.org/hco/6/GRCh38#56955914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#33946231-A-C

56955942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: 33946204-A-G

56956054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: 33946086-G-C

56956281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945894-T-C

56956281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945894-T-G

56956503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945701-A-G

56956520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945681-A-G

56956668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945543-C-G

56956733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945479-G-T

56956747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945465-T-C

56956816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945380-G-C

http://identifiers.org/hco/6/GRCh38#56956903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33945301-A-C

56956903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945301-A-G

56956911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945293-G-A

56957109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33945094-T-A

56957562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33944650-T-G

56957621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33944588-C-T

56957955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33944279-A-G

56958121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33944133-A-G

56958277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33943253-G-A

56958409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33943125-C-G

56958409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33943125-C-T

56958415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33943119-A-G

56958753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33942834-A-G

56958978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33942584-G-T

56959206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33942175-C-T

56959268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33942118-T-C

http://identifiers.org/hco/6/GRCh38#56959457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#33940046-A-C

56959588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33939922-C-G

56959599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33939911-T-C

56959768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33939750-T-C

56959849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: 33939662-C-T

56960022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: 33939549-G-A

56960179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: 33939413-G-C

56960245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33939346-T-C

56960379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: 33939223-C-T

56960524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33938798-G-A

56960524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33938798-G-T

56960923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33938426-T-C

56962332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33937670-A-T

56962376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33937626-C-T

56962526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33937431-A-G

56962543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33937414-C-T

56962602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33937362-C-G

56962833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33936736-G-C

56962854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33936715-G-A

56964823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33935934-C-T

56965220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33935035-G-C

56965252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33935006-G-T

56965766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33934818-T-C

56966132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33934492-T-C

56966325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33934353-C-T

56967069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33933595-T-A

http://identifiers.org/hco/6/GRCh38#56967070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33933594-C-A

56967072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33933592-A-G

56967122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33933554-G-A

56967145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33933531-A-G

56967206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33933419-G-A

56967619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33932990-T-G

56967635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33932974-C-T

56967669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33932943-G-A

56967671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33932941-C-T

http://identifiers.org/hco/6/GRCh38#56967894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33932779-A-C

56967960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33932725-T-C

56968003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33932637-T-G

56968198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33932455-A-G

56969645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33931488-T-C

56969852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33931291-T-C

56970972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33930316-C-T

http://identifiers.org/hco/6/GRCh38#56980724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33923948-A-C

56980773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33923900-T-A

56980777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33923896-A-G

56980895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33923778-G-A

56981291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33923597-T-C

56981361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33923525-T-C

56981745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33922704-G-A

56981745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33922704-G-C

56981760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33922689-G-A

56981760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33922689-G-T

56981770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33922680-C-G

56981772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33922678-C-T

56981775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5 prime UTR variant
orthologous variants: 33922675-A-G

56981889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: missense variant
orthologous variants: 33922561-A-G

56981913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: missense variant
orthologous variants: 33922537-G-A

56981919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: missense variant
orthologous variants: 33922531-G-A

56981939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33922511-T-G

56981950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33922505-G-T

http://identifiers.org/hco/6/GRCh38#56981976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33922473-C-A

56981976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33922473-C-T

56981987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33922462-G-T

56981988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33922461-G-A

56981988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33922461-G-T

56981995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33922452-T-A

56981995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33922452-T-C

56982340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33922238-A-G

56982665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33922003-A-G

56983107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33921898-A-T

56991185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33918375-G-T

56991777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33918002-T-G

56991813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917966-C-T

56991821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917958-A-G

56991873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917906-A-G

http://identifiers.org/hco/6/GRCh38#56991878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33917901-C-A

56991914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917868-G-A

56991948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917843-A-G

56992101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917784-T-C

http://identifiers.org/hco/6/GRCh38#56992226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33917672-C-A

56992226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917672-C-G

http://identifiers.org/hco/6/GRCh38#56992229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33917669-C-A

56992229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917669-C-T

56992233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917665-A-T

56992247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917651-G-A

56992247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917651-G-T

56992305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917596-G-A

56992305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917596-G-C

56992305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917596-G-T

56992306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917595-C-G

http://identifiers.org/hco/6/GRCh38#56992339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33917558-C-A

56992367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917527-T-G

http://identifiers.org/hco/6/GRCh38#56992508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33917386-C-A

56992508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: missense variant
orthologous variants: 33917386-C-G

56992564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917329-T-C

http://identifiers.org/hco/6/GRCh38#56992657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33917235-C-A

56992657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917235-C-T

56992661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917231-G-A

56992744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917167-T-C

56992744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917167-T-G

56992746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917165-T-C

56992851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33917068-G-T

56992959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33916963-T-G

56993210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33916778-T-C

56993243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33916745-G-T

56993256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33916731-A-T

56993349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33916226-A-G

56993635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33915949-G-A

56994039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33915872-G-A

56994142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33915781-A-G

56994151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33915772-G-A

http://identifiers.org/hco/6/GRCh38#56994188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33915736-A-C

56994188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33915736-A-G

57012188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33906395-C-T

57012192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33906391-C-T

57012251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33906314-G-T

http://identifiers.org/hco/6/GRCh38#57012306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33906268-C-A

57012315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33906259-G-C

57012517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33906129-C-T

http://identifiers.org/hco/6/GRCh38#57012807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33905882-A-C

57012925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33905769-C-T

57012991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33905702-T-C

http://identifiers.org/hco/6/GRCh38#57014413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33904409-C-A

57014413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33904409-C-G

http://identifiers.org/hco/6/GRCh38#57014431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33904391-C-A

57014442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33904380-A-G

57014463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 33904359-A-T

http://identifiers.org/hco/6/GRCh38#57014466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33904356-C-A

57014466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33904356-C-T

57014503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33904323-G-A

57014518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33904309-T-C

57014568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33904266-T-C

http://identifiers.org/hco/6/GRCh38#57014603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33904231-C-A

57014631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33904203-A-T

http://identifiers.org/hco/6/GRCh38#57014655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33904179-C-A

57014655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33904179-C-T

57015205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33903750-C-G

57015205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33903750-C-T

57015210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33903745-T-C

57015219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33903736-G-T

http://identifiers.org/hco/6/GRCh38#57015447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33903507-C-A

57015469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903485-T-C

57015486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903468-A-G

57015487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903453-T-G

57015519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903392-G-A

57015551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903359-A-G

57015574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903336-G-T

http://identifiers.org/hco/6/GRCh38#57015625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33903269-C-A

57015625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903269-C-G

http://identifiers.org/hco/6/GRCh38#57017064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33903140-A-C

57017070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903134-T-A

57017070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903134-T-C

57017071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903133-A-G

57017071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903133-A-T

57017077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903127-A-G

57017077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903127-A-T

http://identifiers.org/hco/6/GRCh38#57017160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33903061-A-C

57017160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903061-A-G

57017160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33903061-A-T

57017357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33902863-G-A

57017467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33902753-G-A

57017972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33902203-T-C

http://identifiers.org/hco/6/GRCh38#57018039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33902191-A-C

57018039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33902191-A-G

57018313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33901943-A-G

http://identifiers.org/hco/6/GRCh38#57018442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33901831-C-A

http://identifiers.org/hco/6/GRCh38#57018507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33901766-C-A

57018507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, missense_variant
orthologous variants: 33901766-C-T

57018546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron_variant, undefined
orthologous variants: 33901727-T-C

57018553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33901720-T-C

57018569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901704-A-G

57018569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901704-A-T

57018589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901684-G-A

57018589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901684-G-T

57018616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901666-A-T

57018635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901647-T-C

http://identifiers.org/hco/6/GRCh38#57018638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33901644-C-A

57018638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901644-C-T

57018640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901642-A-G

57018647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901635-T-A

57021418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901083-C-T

57021463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33901035-A-G

57021597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33900888-G-C

57021610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33900868-T-C

57021730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33900755-T-C

57021751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33900734-G-A

57026071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: intron variant
orthologous variants: 33892463-G-T

57026233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3 prime UTR variant
orthologous variants: 33892341-G-A

57026233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3 prime UTR variant
orthologous variants: 33892341-G-T

57026319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3 prime UTR variant
orthologous variants: 33892277-A-G

http://identifiers.org/hco/6/GRCh38#57026654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#33891968-C-A

57026660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3 prime UTR variant
orthologous variants: 33891962-T-C

57026784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3 prime UTR variant
orthologous variants: 33891841-G-T

57026851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3 prime UTR variant
orthologous variants: 33891777-A-G

57026892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20871
most severe consequence: 3 prime UTR variant
orthologous variants: 33891740-T-A