http://identifiers.org/hco/17/GRCh38#1934966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75158339-C-A

1934992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75158314-T-C

http://identifiers.org/hco/17/GRCh38#1935045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75158272-C-A

1935045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75158272-C-T

http://identifiers.org/hco/17/GRCh38#1935292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75158043-C-A

1935292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75158043-C-G

http://identifiers.org/hco/17/GRCh38#1935314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75158028-C-A

http://identifiers.org/hco/17/GRCh38#1935335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75158022-C-A

1935402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157955-G-A

1935402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157955-G-T

http://identifiers.org/hco/17/GRCh38#1935568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75157802-C-A

1935568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157802-C-G

http://identifiers.org/hco/17/GRCh38#1935581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75157789-C-A

1935663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157696-A-G

1936070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157319-G-T

1936176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157222-G-A

1936176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157222-G-C

1936176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157222-G-T

http://identifiers.org/hco/17/GRCh38#1936253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75157149-C-A

1936285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157126-C-T

http://identifiers.org/hco/17/GRCh38#1936294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75157117-A-C

http://identifiers.org/hco/17/GRCh38#1936308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75157104-C-A

1936308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157104-C-T

1936324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157088-C-T

1936354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75157058-T-C

1936422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75156998-G-A

1936422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75156998-G-T

1936487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 3 prime UTR variant
orthologous variants: 75156914-C-T

1936538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: synonymous variant
orthologous variants: 75156863-G-A

1936538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: synonymous variant
orthologous variants: 75156863-G-C

1936538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: synonymous variant
orthologous variants: 75156863-G-T

1936549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: synonymous variant
orthologous variants: 75156852-G-A

1936549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75156852-G-T

1936563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75156838-G-A

1936563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75156838-G-T

1936618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75156783-C-T

http://identifiers.org/hco/17/GRCh38#1936702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75156699-C-A

1936702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75156699-C-T

1936704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75156697-T-C

1936734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75156667-T-C

1936971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75156418-G-A

1936971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75156418-G-T

http://identifiers.org/hco/17/GRCh38#1937394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75155995-C-A

1937400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75155989-G-A

1937436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: missense variant
orthologous variants: 75155953-G-T

1937795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: synonymous variant
orthologous variants: 75155594-C-T

1937855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75155536-G-A

1937855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75155536-G-T

1938220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75155244-T-A

1939735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75154705-C-G

1939735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75154705-C-T

1939796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75154644-C-T

1940202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75154227-C-T

1940377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75154052-C-T

1940700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75153825-C-T

1940949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75153626-G-A

http://identifiers.org/hco/17/GRCh38#1941057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75153536-A-C

1941240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75153418-G-C

1941263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75153396-A-G

1941698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75153003-A-G

1941720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75152981-A-T

1942218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75152515-C-T

1942375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75152380-G-A

1942380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75152375-A-G

1942383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75152372-C-T

1942402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75152353-T-C

1942402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75152353-T-G

1942403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75152352-G-A

1942403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75152352-G-T

http://identifiers.org/hco/17/GRCh38#1942600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75152166-C-A

1942823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75151983-A-T

1942953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75151873-A-T

1943162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75151693-C-T

1943245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75151617-A-G

1943245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75151617-A-T

1943319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75151541-G-C

1943786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75151142-C-T

1948282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75148055-T-C

http://identifiers.org/hco/17/GRCh38#1948361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75147973-C-A

1949508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75147419-A-T

http://identifiers.org/hco/17/GRCh38#1949726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75147196-C-A

1949726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75147196-C-T

1957362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75143130-T-G

1958673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75142591-C-G

1959055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75142237-T-A

1959121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75142176-C-G

1959964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75141648-C-T

1960046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75141563-T-G

1960303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75141350-C-G

1960611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75140983-C-G

1960758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75140824-C-T

http://identifiers.org/hco/17/GRCh38#1960779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75140803-A-C

1960943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75140640-C-G

1961257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75140400-C-G

1961257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75140400-C-T

1961316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75140365-G-A

1961520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75140207-T-C

1961527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75140200-C-T

1963268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75139825-C-T

1963315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75139777-C-G

1963445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75139641-C-G

1963445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75139641-C-T

1965598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75136907-C-T

1965727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75136770-T-C

1966054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75136459-C-T

1966420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75136103-G-A

http://identifiers.org/hco/17/GRCh38#1966523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75135993-A-C

1966523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75135993-A-G

1966592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75135926-G-A

1966603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75135914-C-G

1966603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75135914-C-T

http://identifiers.org/hco/17/GRCh38#1966774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75135791-C-A

1967538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75135209-C-T

1967978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75135093-A-T

1967979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75135092-G-A

1967979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75135092-G-C

1968266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75134797-C-T

1968536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75134503-T-A

http://identifiers.org/hco/17/GRCh38#1968587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75134447-A-C

1968628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75134408-C-T

1968876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75134065-T-C

1968965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75133980-C-T

http://identifiers.org/hco/17/GRCh38#1970544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75131607-A-C

1970605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75131554-C-T

1972799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75129615-C-T

1975022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75128325-G-A

1975068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75128277-C-T

1975388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75128020-T-A

1976151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75127458-A-G

1976219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75127384-G-A

1976551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75127067-A-G

1977224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75126379-G-A

http://identifiers.org/hco/17/GRCh38#1977399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75126221-C-A

1977650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75125981-G-A

1977872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75125759-G-A

1977998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75125730-G-A

1978217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75125586-C-G

1978217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75125586-C-T

1978262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75125540-C-T

1978506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75125311-C-T

1978697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75125095-G-A

1978697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75125095-G-C

1984568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75121217-G-A

1984627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75121157-C-T

1984635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75121149-A-G

1985200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75120952-T-G

1985216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75120936-G-A

1985264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75120887-C-T

1985900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75120253-G-T

1985969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75120184-T-G

1986078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75120066-T-C

1986126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75120017-C-T

1986128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75120015-G-A

1986128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75120015-G-C

1986176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75119986-T-C

1987756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75116505-C-G

1987810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75116450-T-C

1990897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75111947-C-T

1990898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75111946-G-A

1990899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75111945-G-T

1991287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75111538-G-A

1991287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75111538-G-T

1991403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75111418-C-T

1991923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110904-T-C

1992427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110771-A-G

1992683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110512-C-T

1992803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110392-C-T

1992815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110380-A-G

1992869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110325-A-G

1992965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110170-G-A

1992966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110169-G-A

1992968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110167-C-T

1993005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110125-G-A

1993016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110114-G-A

1993022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75110103-C-T

1993402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75109865-T-C

1993476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75109791-T-C

http://identifiers.org/hco/17/GRCh38#1993579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75109698-A-C

http://identifiers.org/hco/17/GRCh38#1993618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75109659-C-A

1993618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75109659-C-T

1994170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75108690-A-G

1995263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75107703-T-A

1995263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75107703-T-C

1995294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75107678-T-C

1995307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75107675-C-G

1995307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75107675-C-T

1995445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75107486-A-G

1995447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75107484-G-A

1995585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75107214-G-C

1995585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75107214-G-T

1995644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75107163-A-G

http://identifiers.org/hco/17/GRCh38#1995651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75107156-C-A

1995736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75107073-T-A

1995791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75107018-A-G

1995809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75107000-G-A

1995809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75107000-G-T

1996106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75106710-G-A

1996214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75106601-T-C

1996261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75106555-C-T

1996551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75106291-A-G

1997067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75105789-C-T

1997232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75105637-G-A

1997232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75105637-G-C

http://identifiers.org/hco/17/GRCh38#1997235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75105634-A-C

1997749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75105179-C-G

http://identifiers.org/hco/17/GRCh38#1997830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75105090-A-C

http://identifiers.org/hco/17/GRCh38#1997959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75104977-C-A

1997980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75104956-C-G

1998093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75104845-G-A

1998185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75104754-C-G

1998315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75104615-C-G

http://identifiers.org/hco/17/GRCh38#1998467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75104509-C-A

http://identifiers.org/hco/17/GRCh38#1998747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75104281-C-A

1998747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75104281-C-G

1998807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75104245-G-A

http://identifiers.org/hco/17/GRCh38#1999660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75103487-A-C

1999673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75103470-G-C

1999711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75103411-T-C

1999711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75103411-T-G

2000274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75102875-G-A

2001543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75102084-G-A

2001543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75102084-G-T

2001551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75102076-T-A

2001551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75102076-T-C

2001553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75102074-A-G

2001554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75102073-T-A

2001554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75102073-T-C

2001673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101955-C-G

2001673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101955-C-T

2001916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101736-C-G

http://identifiers.org/hco/17/GRCh38#2001917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75101735-A-C

2001926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101726-C-G

2001926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101726-C-T

2001955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101707-G-A

2002766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101365-G-A

2002766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101365-G-C

2002766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101365-G-T

2002791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101350-G-A

2002806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101331-G-A

2002884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101247-G-T

2002891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101240-G-A

2002891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101240-G-T

2003110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101062-G-A

2003110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75101062-G-T

2003201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75100980-G-A

http://identifiers.org/hco/17/GRCh38#2003205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75100976-C-A

2003205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75100976-C-T

http://identifiers.org/hco/17/GRCh38#2003234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75100947-C-A

2003234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75100947-C-T

http://identifiers.org/hco/17/GRCh38#2003236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75100945-C-A

2003342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75100842-A-G

2003342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75100842-A-T

http://identifiers.org/hco/17/GRCh38#2003405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75100804-C-A

2003405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75100804-C-T

http://identifiers.org/hco/17/GRCh38#2003521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75100710-C-A

2003671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75100517-G-A

2003723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75100472-A-G

2003785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75100411-T-A

2003785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75100411-T-C

2007123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75099079-G-A

2007264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75098947-C-T

http://identifiers.org/hco/17/GRCh38#2007335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75098874-C-A

2007374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75098835-A-T

2007816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75098497-C-T

2007897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75098423-G-T

http://identifiers.org/hco/17/GRCh38#2008352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75097877-A-C

2008352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75097877-A-G

2008439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75097805-G-T

2008679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75097553-G-A

2008895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75097314-T-C

2008896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75097313-C-T

2008968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75097245-C-T

2009643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75096879-C-T

2009923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75096635-T-A

2011390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75096009-C-G

2011390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75096009-C-T

2011460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75095921-G-A

2011541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75095813-G-A

2011603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75095766-G-A

2011608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75095761-T-C

2011621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75095753-T-G

2011622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75095752-C-T

2011964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75095445-C-G

2012072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75095336-G-A

2012081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75095327-T-C

2013925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75094908-C-T

2014095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75094746-G-A

2014141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75094699-G-A

2014552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75094333-C-T

2014555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75094330-G-C

http://identifiers.org/hco/17/GRCh38#2015023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75094075-A-C

2015050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75094048-T-C

2015261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093847-C-T

2015267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093841-G-A

2015272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093836-G-C

2015335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093712-C-T

2015391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093661-C-G

2015391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093661-C-T

2015488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093575-C-T

2015523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093536-A-G

2015588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093456-C-T

2015697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093414-T-G

2015732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093375-C-T

2015733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093374-C-G

2015733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093374-C-T

2015806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093295-T-A

2015967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093143-C-T

2015983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093127-G-A

2016001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75093109-C-T

2016481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75092940-G-C

http://identifiers.org/hco/17/GRCh38#2016574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75092842-A-C

2016582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75092834-G-A

2016758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75092670-C-T

2016761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75092667-C-T

2017055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75092382-C-T

2017239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75092218-C-T

2017246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75092211-T-G

2017542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091902-C-T

2017566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091879-G-T

2017669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091783-G-T

2017710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091722-C-G

2017710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091722-C-T

2017755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091665-T-C

2017824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091596-G-C

2017824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091596-G-T

2017826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091594-T-C

2017887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091515-G-C

http://identifiers.org/hco/17/GRCh38#2018049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75091404-C-A

2018079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091374-G-T

http://identifiers.org/hco/17/GRCh38#2018194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75091228-C-A

http://identifiers.org/hco/17/GRCh38#2018217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75091211-C-A

2018217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091211-C-T

2018242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091186-C-T

2018245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091183-G-A

2018245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091183-G-T

2018423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75091017-A-T

2018642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75090849-G-A

2018693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75090643-T-C

2018869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75090429-G-A

2018869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75090429-G-T

http://identifiers.org/hco/17/GRCh38#2018870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75090428-C-A

2018870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75090428-C-T

2018955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75090338-G-C

2019038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75090233-C-G

http://identifiers.org/hco/17/GRCh38#2019081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75090193-C-A

2019081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75090193-C-G

2019192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75089895-C-T

2019202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75089885-A-G

2019205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75089882-C-T

2019261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75089826-T-C

http://identifiers.org/hco/17/GRCh38#2019381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75089707-C-A

http://identifiers.org/hco/17/GRCh38#2019403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75089685-C-A

2019403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75089685-C-T

2019493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75089595-A-G

http://identifiers.org/hco/17/GRCh38#2019855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75089230-C-A

2019855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75089230-C-T

2019896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75089192-G-A

2019896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75089192-G-T

2019978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75088877-G-T

2020033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75088824-T-G

2020060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75088797-C-T

http://identifiers.org/hco/17/GRCh38#2020081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75088771-A-C

2020081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75088771-A-G

http://identifiers.org/hco/17/GRCh38#2020131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75088722-C-A

http://identifiers.org/hco/17/GRCh38#2020220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75088622-C-A

http://identifiers.org/hco/17/GRCh38#2020256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75088589-C-A

2020323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75088530-C-T

2020381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75088472-G-T

2020452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75088407-C-G

2020847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75088009-T-C

2020923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75087936-C-T

http://identifiers.org/hco/17/GRCh38#2020985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75087872-C-A

2020985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75087872-C-G

2021093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75087770-C-G

2022629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75087309-A-T

2022636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75087302-G-A

2022826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75087111-G-C

2022915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75087045-C-G

2022988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086974-G-A

2022988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086974-G-C

2023425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086526-C-G

2023425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086526-C-T

2023435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086516-T-C

2023546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086394-G-C

2023546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086394-G-T

2023620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086327-T-A

2023620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086327-T-C

http://identifiers.org/hco/17/GRCh38#2023624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75086323-C-A

2023624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086323-C-T

http://identifiers.org/hco/17/GRCh38#2023638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75086307-C-A

2023638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086307-C-T

2023644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086301-G-A

2023644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086301-G-T

2023664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086282-T-C

2023664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086282-T-G

2023666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086280-C-T

http://identifiers.org/hco/17/GRCh38#2023677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#75086269-C-A

2023856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75086115-C-T

2024072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75085897-T-A

2024087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron_variant, undefined
orthologous variants: 75085882-G-T

2024103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75085866-C-G

2024103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75085866-C-T

2024537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75085443-C-T

http://identifiers.org/hco/17/GRCh38#2024738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75085233-C-A

2024738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: intron variant
orthologous variants: 75085233-C-T

http://identifiers.org/hco/17/GRCh38#2024913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75085058-C-A

2024913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: 75085058-C-T

http://identifiers.org/hco/17/GRCh38#2024982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75084989-C-A

2024982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: 75084989-C-G

2024982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: 75084989-C-T

2025025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: 75084946-T-C

2025153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: 75084819-G-A

2025153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: 75084819-G-C

2025153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: 75084819-G-T

2025214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: 75084758-G-A

http://identifiers.org/hco/17/GRCh38#2025275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#75084706-C-A

2025275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: 75084706-C-T

2025286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21329
most severe consequence: 5 prime UTR variant
orthologous variants: 75084695-C-T