82979623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73632853-G-A

http://identifiers.org/hco/9/GRCh38#82979919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73633151-C-A

82979990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73633218-A-G

82979991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73633219-T-A

82980113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73633338-G-A

82980361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73633580-A-G

82980500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73633696-G-A

82980737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73633904-G-T

82980886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73634074-T-C

82980996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73634153-A-G

82981139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73634500-G-C

82981139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73634500-G-T

82981252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73634651-C-T

82981456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73634854-G-A

82981597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73634984-T-C

82981666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73635054-G-C

82981703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73635072-C-T

82981742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73635108-A-G

http://identifiers.org/hco/9/GRCh38#82981781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73635142-C-A

82981850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 3 prime UTR variant
orthologous variants: 73635200-G-A

82982755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73635983-A-G

82982788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73636016-A-G

82982788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 73636016-A-T

82986559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73638198-C-G

http://identifiers.org/hco/9/GRCh38#82987768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73641310-C-A

82987768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73641310-C-T

82987786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73641328-T-G

82989019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73642913-C-T

82989080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73642982-C-G

82989081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73642983-A-G

82989110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73643027-G-A

82990144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73645137-G-A

http://identifiers.org/hco/9/GRCh38#82990183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73645184-C-A

82990230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73645643-G-A

82990233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73645646-G-T

82990301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73645703-G-A

82990301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73645703-G-T

82990380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73645795-C-T

82990484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73645899-C-T

82990500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73645915-G-A

82990500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73645915-G-T

82990513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73645928-T-C

82990696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73646450-T-C

82990696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73646450-T-G

82990733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73646486-G-C

82990862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73646691-C-T

82990946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73646760-T-C

82991094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73646900-C-T

82991202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73647073-C-T

82991357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73647202-T-C

82992431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73649244-A-T

82992439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73649252-A-G

82992566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73649375-A-G

http://identifiers.org/hco/9/GRCh38#82992733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73649532-A-C

82992914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73649669-G-A

http://identifiers.org/hco/9/GRCh38#82992993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73649748-C-A

82992993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73649748-C-T

http://identifiers.org/hco/9/GRCh38#82993014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73649769-A-C

82993014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: 73649769-A-T

http://identifiers.org/hco/9/GRCh38#82993070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73649823-C-A

82993070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73649823-C-T

82993351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73650189-G-T

82993461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73650268-G-A

82993461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73650268-G-C

82993517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73650326-G-A

82993576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73650384-G-T

82994296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73650910-T-C

82994399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73651000-T-A

http://identifiers.org/hco/9/GRCh38#82994556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73651176-C-A

82994556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73651176-C-G

82994560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73651180-G-A

82995827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73651696-T-C

82995827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73651696-T-G

82996327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73652143-A-G

82996404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73652201-A-G

82996475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73652258-C-G

82996475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73652258-C-T

82996598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73652349-G-A

82996844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73652561-G-A

82996909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73652589-G-A

82996909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73652589-G-C

82996909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73652589-G-T

http://identifiers.org/hco/9/GRCh38#82997240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73652912-C-A

82997240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73652912-C-G

82997406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73653021-G-A

82997972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73653600-G-A

82998092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73653707-G-T

82998229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73653840-A-G

82998246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73653862-G-A

82998246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73653862-G-T

http://identifiers.org/hco/9/GRCh38#82998346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73653938-C-A

82998346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73653938-C-T

http://identifiers.org/hco/9/GRCh38#82998576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73654124-C-A

82998624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73654161-G-A

82998624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73654161-G-C

82998889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73654465-T-C

82998944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73654547-G-A

82998957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73654571-C-T

83000164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73658480-C-T

83000335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73658649-G-C

83000381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73658688-G-A

83000437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: 73658727-G-A

83000448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73658738-T-C

83000480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: 73658770-T-C

83000763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73659029-A-G

83000791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73659057-A-G

http://identifiers.org/hco/9/GRCh38#83000808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73659096-C-A

83000853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73659128-A-G

83000853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73659128-A-T

83000938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73659209-G-A

83000938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: 73659209-G-C

http://identifiers.org/hco/9/GRCh38#83001146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73659414-A-C

http://identifiers.org/hco/9/GRCh38#83001187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73659455-C-A

83001187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73659455-C-T

83001249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73659503-G-T

83001274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73659519-G-C

83001274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73659519-G-T

83001280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73659525-T-C

83003963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73661862-T-C

83004063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73661960-T-C

83004256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73662049-A-G

83004408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73662207-T-A

83004408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73662207-T-C

83004408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73662207-T-G

83004507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: 73662305-C-G

83004507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: 73662305-C-T

83004533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73662331-G-A

83004533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: 73662331-G-T

http://identifiers.org/hco/9/GRCh38#83004647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73662425-C-A

83004647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73662425-C-T

http://identifiers.org/hco/9/GRCh38#83004666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73662444-C-A

83004666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73662444-C-T

83005000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73662762-G-C

83005241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73663094-T-C

83005274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73663127-C-T

83005315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73663168-T-C

83005344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73663192-A-G

83005358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73663204-C-T

83005489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: 73663335-C-G

83005489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: 73663335-C-T

83005531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73663372-G-C

83005531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73663372-G-T

83005850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73665406-T-C

83006338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73665926-G-T

83006381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73665990-C-T

83006463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73666074-T-C

83006585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73666193-A-G

83006616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73666219-G-T

83006864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73666404-C-T

83007296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73666678-G-A

83007296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73666678-G-T

83007368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73666737-G-A

83007368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73666737-G-C

83007368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73666737-G-T

83007517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73666879-T-C

83008601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73667321-G-A

83008782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73667444-C-G

http://identifiers.org/hco/9/GRCh38#83008787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73667449-C-A

83008787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73667449-C-T

83008793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73667455-C-G

83008906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73667559-A-G

83009137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73667704-T-C

83009326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73667875-C-T

83009328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73667877-G-T

83009533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73668034-T-C

83009536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73668037-T-G

83009587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73668067-G-C

83009587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73668067-G-T

83009667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73668106-A-G

http://identifiers.org/hco/9/GRCh38#83009694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73668133-A-C

83011686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73676514-T-C

83011712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73676917-C-T

83011838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73677033-A-G

83011838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73677033-A-T

83012238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73677362-G-A

83012406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73677905-T-C

83012419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73677917-A-G

83012419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73677917-A-T

83012422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73677919-G-T

83012424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73677921-T-C

83012467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73677964-A-G

83012500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73677997-T-C

http://identifiers.org/hco/9/GRCh38#83012521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73678018-C-A

83012521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73678018-C-T

83012559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73678030-G-C

83012559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73678030-G-T

83012570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73678041-G-C

83012570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73678041-G-T

http://identifiers.org/hco/9/GRCh38#83012623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#73678094-C-A

83012623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73678094-C-T

83012642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73678113-A-T

83012679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73678149-A-G

http://identifiers.org/hco/9/GRCh38#83012701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73678171-C-A

83012714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73678181-G-A

83012830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73678287-A-T

83013304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73679197-G-A

83013460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73679682-C-T

http://identifiers.org/hco/9/GRCh38#83013545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73679769-A-C

83013750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73679976-T-C

83013813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73680034-G-A

83015862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73681161-T-C

83015872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: missense variant
orthologous variants: 73681171-C-G

83015962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73681261-C-T

83015989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73681288-A-G

83015989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73681288-A-T

http://identifiers.org/hco/9/GRCh38#83015996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73681294-C-A

83015996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73681294-C-T

http://identifiers.org/hco/9/GRCh38#83016138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73681429-C-A

83016191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73681476-A-G

83020373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73686476-C-T

83020420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73686521-C-T

83020427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73686528-G-A

83020637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73686724-A-T

83020783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73686865-G-A

83020814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73686898-T-C

83020863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73686944-G-A

83021093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73687173-G-A

83021130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73687198-C-G

83021147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73687215-C-T

83021168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73687232-C-T

83021217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73687282-G-A

83021217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73687282-G-T

http://identifiers.org/hco/9/GRCh38#83021316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73687373-A-C

83022002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73687669-G-A

http://identifiers.org/hco/9/GRCh38#83022234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73687925-C-A

83022265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73687957-G-C

83022265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73687957-G-T

83022296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73687988-A-G

83022423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73688119-G-A

83022423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: synonymous variant
orthologous variants: 73688119-G-T

http://identifiers.org/hco/9/GRCh38#83022567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73688238-C-A

83022567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73688238-C-T

83023061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73688343-T-C

83023111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73688386-G-T

83023190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73688462-A-G

http://identifiers.org/hco/9/GRCh38#83025674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73689431-C-A

83025702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689459-G-T

83025711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689468-C-T

83025822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 73689570-G-A

83025822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 73689570-G-C

83025858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 73689606-T-C

http://identifiers.org/hco/9/GRCh38#83025943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73689692-A-C

83025981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689729-G-A

83025981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689729-G-T

http://identifiers.org/hco/9/GRCh38#83026007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73689750-A-C

83026007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689750-A-G

83026008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689751-T-A

83026008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689751-T-C

83026067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689805-G-A

83026067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689805-G-T

83026104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689838-G-T

83026266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73689958-T-C

83026745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73690057-T-A

83026751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73690063-A-G

83027326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73690573-C-G

83027440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73690716-T-C

83027484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73690739-A-G

83027507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73690762-G-C

83027811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73691163-G-A

83027874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73691288-T-C

http://identifiers.org/hco/9/GRCh38#83027936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73691356-C-A

83028114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73691535-T-C

83028335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73691757-T-A

83029136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73693760-C-T

http://identifiers.org/hco/9/GRCh38#83029143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73693765-A-C

83029304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73693882-A-T

83029332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73693910-C-T

83029787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73694051-A-G

83029901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73694159-C-T

83030024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73694289-A-G

83030641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73694601-G-C

http://identifiers.org/hco/9/GRCh38#83030656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73694613-A-C

83032048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73694951-C-T

83032170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73695040-G-A

83032211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73695081-G-A

83032234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73695104-A-G

83032376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73695222-C-T

83032384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73695230-C-T

83032385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73695231-T-C

83032751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73695855-C-T

83033217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73696322-G-A

83033383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73696467-A-G

83033392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73696476-C-T

83034330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73696533-C-T

83034338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73696541-T-C

83034406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73696601-C-T

83034436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73696625-T-G

83034815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73696973-C-T

83059824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73704826-C-T

83060126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73705596-T-C

http://identifiers.org/hco/9/GRCh38#83060146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73705611-C-A

83060304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73705762-A-T

http://identifiers.org/hco/9/GRCh38#83061208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73707912-A-C

83061395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73708081-A-G

83061874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73708465-C-T

http://identifiers.org/hco/9/GRCh38#83061936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73708511-A-C

83062114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73708667-C-T

83062295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73708802-A-G

http://identifiers.org/hco/9/GRCh38#83062546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73708979-C-A

83062546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, missense_variant
orthologous variants: 73708979-C-T

83062549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, missense_variant
orthologous variants: 73708982-C-T

83062643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 73709007-G-A

83062643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 73709007-G-C

83062643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 73709007-G-T

83062714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, stop_gained
orthologous variants: 73709078-G-A

83062714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, missense_variant
orthologous variants: 73709078-G-T

http://identifiers.org/hco/9/GRCh38#83062745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73709109-C-A

83062745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 73709109-C-T

83062762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 73709126-G-A

83062762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, missense_variant
orthologous variants: 73709126-G-C

83062762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, missense_variant
orthologous variants: 73709126-G-T

83062768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, missense_variant
orthologous variants: 73709132-G-A

83062768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 73709132-G-T

83062918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73709259-G-A

83062919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73709260-G-A

83062919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73709260-G-T

83062980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73709288-C-T

83063103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73709356-C-G

83063103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73709356-C-T

83063129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73709378-C-T

http://identifiers.org/hco/9/GRCh38#83063150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#73709398-C-A

83063150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 73709398-C-G

83063214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron variant
orthologous variants: 73709452-A-G

83063438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73709662-C-T

83063458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73709688-T-C

83063542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73709775-A-G

83063680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73709865-G-C

83064217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73712656-T-G

83064261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73712717-C-T

83064536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73712971-C-G

http://identifiers.org/hco/9/GRCh38#83064542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#73712977-C-A

83065117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73713195-T-A

83065260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73713351-T-A

83065336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73713408-T-C

83065339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73713411-A-G

83065377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26464
most severe consequence: intron_variant, undefined
orthologous variants: 73713423-T-C