80537904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615333-T-C

80537914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615323-C-G

http://identifiers.org/hco/10/GRCh38#80537922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40615315-C-A

80537922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615315-C-G

80537922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615315-C-T

80537924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615313-A-T

80538024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615237-T-C

80538034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615227-T-G

http://identifiers.org/hco/10/GRCh38#80538041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40615220-C-A

80538041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615220-C-T

80538046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615207-T-C

80538097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615152-G-A

80538113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615146-T-C

80538120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615139-T-A

80538120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615139-T-C

80538120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615139-T-G

http://identifiers.org/hco/10/GRCh38#80538167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40615095-C-A

80538167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615095-C-T

80538210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615052-A-G

80538212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615050-G-T

80538224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615038-T-A

80538224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615038-T-C

80538224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615038-T-G

80538253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615012-G-A

80538253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40615012-G-T

http://identifiers.org/hco/10/GRCh38#80538294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40614955-C-A

80538294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40614955-C-T

80538305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40614944-T-C

80538314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 5 prime UTR variant
orthologous variants: 40614938-T-C

http://identifiers.org/hco/10/GRCh38#80538368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40614884-C-A

80538368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense variant
orthologous variants: 40614884-C-T

http://identifiers.org/hco/10/GRCh38#80538410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40614842-C-A

http://identifiers.org/hco/10/GRCh38#80538437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40614815-C-A

80538437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: synonymous variant
orthologous variants: 40614815-C-T

http://identifiers.org/hco/10/GRCh38#80538497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40614755-C-A

80538497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense variant
orthologous variants: 40614755-C-T

80538530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40614722-G-A

80538530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40614722-G-C

80538530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40614722-G-T

80538540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40614709-G-A

80538540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40614709-G-T

80538566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40614681-A-G

80538575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40614672-A-G

http://identifiers.org/hco/10/GRCh38#80538600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40614647-C-A

80538600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40614647-C-G

80538603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40614644-G-C

80538747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40614516-G-A

80539014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40613667-G-C

80539039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40613642-G-A

80539045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40613636-C-T

80539176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40613504-A-G

80539235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40613456-A-G

http://identifiers.org/hco/10/GRCh38#80539387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40612297-C-A

80539819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611910-T-G

80539907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611784-G-A

80539907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611784-G-C

80539940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611762-C-T

80540349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611347-G-A

80540355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611341-A-G

80540385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611311-G-A

80540396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611300-G-A

80540538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611167-T-G

80540545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611160-C-T

80540674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611015-G-A

80540674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40611015-G-T

http://identifiers.org/hco/10/GRCh38#80540697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#40610992-C-A

http://identifiers.org/hco/10/GRCh38#80540698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#40610991-A-C

80540736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, undefined
orthologous variants: 40610970-G-A

80540766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, undefined
orthologous variants: 40610939-G-A

80540766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, undefined
orthologous variants: 40610939-G-T

http://identifiers.org/hco/10/GRCh38#80540782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40610923-C-A

80540782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40610923-C-T

80541396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40610826-T-A

80541500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40610725-G-A

80541536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, undefined
orthologous variants: 40610689-G-A

80541567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40610659-A-G

80541767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40610500-G-A

80541781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40610486-T-C

http://identifiers.org/hco/10/GRCh38#80541929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40610351-A-C

80550073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40609518-A-G

80550073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40609518-A-T

http://identifiers.org/hco/10/GRCh38#80550255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40609353-A-C

80552537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40607348-G-A

80552623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40607266-G-A

80552669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40607231-C-T

80552690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40607211-A-G

80552745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40607155-T-C

80553300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606966-T-G

80553419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606831-G-T

80553482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606769-G-A

80553616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606688-G-C

80553623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606681-T-C

80553876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606480-G-T

80553936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606419-T-A

http://identifiers.org/hco/10/GRCh38#80553970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40606405-A-C

80554003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606375-C-T

80554036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606340-G-A

http://identifiers.org/hco/10/GRCh38#80554043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40606333-A-C

80554234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606161-G-C

80554301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40606096-G-A

80554410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40605989-C-T

http://identifiers.org/hco/10/GRCh38#80554558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40605901-C-A

80554558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40605901-C-G

80554558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40605901-C-T

80554619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40605850-T-G

80555182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40605405-G-C

80555336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40605243-C-T

80555779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40604209-C-T

80556106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40603943-G-A

80556150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40603900-A-T

80556179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40603847-T-C

80556244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40603774-C-T

80556245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40603773-G-A

80556293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40603730-G-A

80556411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40603600-T-C

80570244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense variant
orthologous variants: 40596107-A-G

80570521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40595179-T-G

80570824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594899-A-G

80570829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594894-T-C

80571320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594767-G-A

80571320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594767-G-T

http://identifiers.org/hco/10/GRCh38#80571371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40594693-A-C

80571371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594693-A-G

http://identifiers.org/hco/10/GRCh38#80571419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40594644-C-A

80571419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594644-C-G

80571602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594461-G-C

http://identifiers.org/hco/10/GRCh38#80571603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40594460-C-A

80571603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594460-C-T

http://identifiers.org/hco/10/GRCh38#80571632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40594444-C-A

80571632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594444-C-T

80571636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594440-G-T

80571648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594428-T-C

80571657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40594419-T-C

80575263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40591475-T-C

80575369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40591311-A-T

80576190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40590396-T-G

80576309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40590275-G-A

80576309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40590275-G-C

80576401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40590190-A-G

80578659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40589225-G-C

80578847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40589070-C-T

80578849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40589068-A-G

80578850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40589067-C-T

80579145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40588807-G-A

80579513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40588229-G-A

80579761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40588066-A-T

80580707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40587323-G-C

80580790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40587251-G-T

80581393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40586642-C-T

80581639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40586436-C-T

80581757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40586331-A-G

80582308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40583895-G-C

80582308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40583895-G-T

80582493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40583700-C-T

http://identifiers.org/hco/10/GRCh38#80582503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40583690-C-A

80582503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40583690-C-T

80582507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40583686-C-T

80582535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40583655-G-A

http://identifiers.org/hco/10/GRCh38#80588510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40582822-C-A

80588510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582822-C-T

http://identifiers.org/hco/10/GRCh38#80588519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40582813-C-A

80588519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582813-C-T

80588575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582748-G-A

80588575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582748-G-T

80588610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582714-C-T

80588651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: stop gained
orthologous variants: 40582673-A-T

80588826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582499-C-G

80588826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582499-C-T

http://identifiers.org/hco/10/GRCh38#80588843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40582482-C-A

80588858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582467-G-A

http://identifiers.org/hco/10/GRCh38#80588878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40582447-C-A

80588878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582447-C-G

http://identifiers.org/hco/10/GRCh38#80588881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40582444-C-A

80588881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582444-C-G

80588881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40582444-C-T

80597985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40575266-G-A

80598344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40575034-G-T

80598396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40574982-G-A

80598396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40574982-G-C

http://identifiers.org/hco/10/GRCh38#80598694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40574674-A-C

80598694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40574674-A-G

80599057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40574345-C-G

80599074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40574328-C-T

80599094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40574309-A-G

80599194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40574202-A-G

http://identifiers.org/hco/10/GRCh38#80599229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40574168-C-A

80601593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40565472-C-T

80601673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40565402-A-G

80601734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40565357-A-G

80601737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40565354-T-C

80603527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40564596-T-C

80603609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense variant
orthologous variants: 40564515-G-A

80603609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense variant
orthologous variants: 40564515-G-T

http://identifiers.org/hco/10/GRCh38#80603722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40564402-C-A

80603851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40564299-G-T

80603913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40564246-T-A

80603913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40564246-T-C

80604052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40564096-G-A

80604109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40564041-A-G

80604118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40564032-C-T

80604123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40564027-A-G

80604173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40563977-G-A

80604475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40563692-A-G

80604524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40563645-C-T

80604525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40563644-T-C

80604564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40563607-C-T

80604585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40563587-C-T

http://identifiers.org/hco/10/GRCh38#80604627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40563509-A-C

80604673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron variant
orthologous variants: 40563460-G-T

http://identifiers.org/hco/10/GRCh38#80609305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40562405-C-A

80609305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562405-C-T

http://identifiers.org/hco/10/GRCh38#80609358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40562362-C-A

80609383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562347-C-G

80609383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562347-C-T

http://identifiers.org/hco/10/GRCh38#80609401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40562330-C-A

80609401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562330-C-T

80609533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40562198-A-G

80609555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562176-G-A

80609555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562176-G-T

80609608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562129-T-C

80609611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562126-G-A

80609611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562126-G-T

80609631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562106-G-A

80609695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562032-A-G

80609695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40562032-A-T

http://identifiers.org/hco/10/GRCh38#80609699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40562028-C-A

80609794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40561937-C-T

80610134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560338-C-T

80610148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560324-C-T

80610172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560300-C-T

80610366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560107-T-G

80610367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560106-G-T

80610384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560088-C-G

80610417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560063-G-A

80610423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40560057-G-A

http://identifiers.org/hco/10/GRCh38#80610575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40559871-A-C

http://identifiers.org/hco/10/GRCh38#80611221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40559566-C-A

80611348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40559445-A-G

80611430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40559367-A-G

80611491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40559311-A-G

80611553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40559257-C-T

http://identifiers.org/hco/10/GRCh38#80612175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40558346-A-C

80612175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40558346-A-T

80612235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40558276-C-T

80613599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40557266-G-A

80613627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40557239-G-T

80615267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40557018-C-G

80615306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40556979-T-G

80615388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40556910-G-C

http://identifiers.org/hco/10/GRCh38#80615860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40556497-C-A

80615860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40556497-C-G

80615881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40556483-A-G

80616057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40556322-A-G

80617240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40554578-C-T

80617271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40554550-G-A

80617271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40554550-G-C

80617727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40553610-G-T

http://identifiers.org/hco/10/GRCh38#80617833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40553527-A-C

80617953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40553408-G-A

80618037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40553332-C-T

80618294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40552856-G-A

80618365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40552700-G-A

80618382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40552691-G-C

http://identifiers.org/hco/10/GRCh38#80618407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40552664-A-C

80618520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40552551-C-T

80618764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40552305-G-A

80618793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40552274-T-C

80619287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40551848-T-C

80619328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40551821-G-T

http://identifiers.org/hco/10/GRCh38#80621603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40548899-C-A

80621603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40548899-C-T

http://identifiers.org/hco/10/GRCh38#80622129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40548528-C-A

80622221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40548423-C-G

80632829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40544221-G-A

80632994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40544040-G-A

80632994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40544040-G-T

80633042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543999-T-G

80633048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543993-A-G

80633444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543745-A-G

80633482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543710-G-C

80633557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543647-G-A

80633696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543497-A-G

80633746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543453-G-A

80634045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543040-G-A

80634045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543040-G-C

80634067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40543018-C-T

http://identifiers.org/hco/10/GRCh38#80634157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40542935-C-A

80634157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542935-C-T

http://identifiers.org/hco/10/GRCh38#80634161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40542927-C-A

80634161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542927-C-G

http://identifiers.org/hco/10/GRCh38#80634162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40542926-C-A

80634162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542926-C-T

80634175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542913-A-G

80634177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542911-G-A

80634177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542911-G-T

http://identifiers.org/hco/10/GRCh38#80634185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40542903-C-A

80634185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542903-C-T

80634191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542897-G-A

80634191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542897-G-C

80634191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542897-G-T

http://identifiers.org/hco/10/GRCh38#80634251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40542836-C-A

80634251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542836-C-G

80634254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542833-T-A

80634284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 40542791-G-A

80634378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 40542697-C-T

80634386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 40542689-T-C

80634452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 40542623-G-A

80634479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 40542596-C-T

80634530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542545-G-A

80634530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542545-G-C

80634530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542545-G-T

80634531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542544-G-A

80634531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542544-G-C

80634531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542544-G-T

80634540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542539-G-A

80634540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542539-G-T

80634543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542536-A-G

80634613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542467-G-A

80634613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542467-G-T

80634778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542307-C-T

80634928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40542180-T-C

80635092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40541061-G-A

80635132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40541022-G-A

http://identifiers.org/hco/10/GRCh38#80635166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40541010-A-C

80635558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540669-C-T

80641686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40540024-G-A

80642979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40538800-G-A

80642979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40538800-G-T

80643320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40538500-T-C

80643320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40538500-T-G

80643344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40538475-G-A

80643344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40538475-G-T

80643457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40538371-C-T

80643985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40537923-T-C

80644008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537900-G-T

80644169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537739-T-G

http://identifiers.org/hco/10/GRCh38#80644188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40537720-A-C

80644212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537696-A-T

http://identifiers.org/hco/10/GRCh38#80644239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40537672-C-A

80644239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537672-C-G

80644239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537672-C-T

80644240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537671-A-T

80644335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537600-A-G

80644361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537574-A-G

80644426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537509-G-T

80644465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537470-A-G

80644569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537375-T-C

80644795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537153-T-A

80644845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537103-T-C

80644851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537097-G-T

80644898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537049-A-T

80644901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537046-G-A

http://identifiers.org/hco/10/GRCh38#80644907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40537040-C-A

80644907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40537040-C-T

80644960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40536993-C-T

80645836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40534185-T-C

http://identifiers.org/hco/10/GRCh38#80645849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#40534172-C-A

80645934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40534087-T-A

80645947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40534076-T-G

80645960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31440
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40534061-T-C