20933135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3 prime UTR variant
orthologous variants: 119521921-T-C

20933295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119522081-G-A

20933538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119522324-G-T

20933841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119522565-A-G

20933925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119522645-T-C

20935220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119523958-G-T

20935228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119523966-T-C

20935273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119524011-T-C

20935283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119524021-G-A

20935314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119524053-C-T

20935317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119524056-C-G

20935328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119524067-C-T

20935344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119524083-C-T

20936491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119525448-C-T

20936620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119525598-G-A

20936620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119525598-G-T

20936865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119525842-G-A

20936865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119525842-G-T

20936877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119525854-G-A

20936877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119525854-G-T

http://identifiers.org/hco/16/GRCh38#20936887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119525864-C-A

20936887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119525864-C-T

20936925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119525900-G-A

20936925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119525900-G-T

20937816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119526905-G-A

20937882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119526961-G-A

20937906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119526985-G-T

20938048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119527115-T-A

20938048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119527115-T-G

20941291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119527817-G-A

20941291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119527817-G-T

20941376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119527901-A-G

20941376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119527901-A-T

20941390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119527915-A-G

20941730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119528226-G-A

20941730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119528226-G-C

20942565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119528648-A-G

http://identifiers.org/hco/16/GRCh38#20944177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119529106-C-A

http://identifiers.org/hco/16/GRCh38#20944400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119529263-C-A

20944400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119529263-C-G

20944400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119529263-C-T

20944537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, undefined
orthologous variants: 119529366-T-G

20944705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119529534-G-T

20944774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119529605-A-G

20944845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119529666-G-C

20944899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119529712-T-C

20948357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119530531-T-C

20948384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119530558-T-A

20948411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119530589-C-T

20948538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense variant
orthologous variants: 119530696-T-C

http://identifiers.org/hco/16/GRCh38#20948594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119530752-C-A

20948650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119530808-A-G

20948664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119530822-T-C

20948698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119530853-T-G

20948779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119530915-G-T

http://identifiers.org/hco/16/GRCh38#20949708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119533632-C-A

20949828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119533738-G-A

20949870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119533768-G-A

20949966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119533860-T-C

20949966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119533860-T-G

20950370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119534041-T-A

20950716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119534351-C-T

http://identifiers.org/hco/16/GRCh38#20951318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119534637-A-C

20951365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119534687-C-T

20952375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119536135-C-G

20952375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119536135-C-T

20952376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119536136-A-T

20952425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119536185-G-A

20952425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119536185-G-T

20952461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119536221-C-T

20952514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119536274-G-A

20952514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense variant
orthologous variants: 119536274-G-C

20952561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119536321-A-T

20952567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119536327-G-T

20952584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119536346-T-C

20952941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119536694-C-T

20954707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119537928-C-T

http://identifiers.org/hco/16/GRCh38#20954714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119537937-C-A

20954714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119537937-C-G

http://identifiers.org/hco/16/GRCh38#20955126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119538323-C-A

20955126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119538323-C-G

20955126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119538323-C-T

20955127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119538324-A-G

20959049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119542542-T-C

20959217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119542722-C-T

20959352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119542857-G-A

20959352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119542857-G-C

20959377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense variant
orthologous variants: 119542882-C-T

20963215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119549746-G-A

20963215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119549746-G-T

20963224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119549755-C-G

20963224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119549755-C-T

http://identifiers.org/hco/16/GRCh38#20963235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119549768-C-A

20963235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119549768-C-T

http://identifiers.org/hco/16/GRCh38#20963441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119549974-A-C

20963441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119549974-A-G

20963474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119550007-C-T

20963528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119550061-C-T

20963557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119550090-G-A

20963749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense variant
orthologous variants: 119550282-T-C

20963978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119550511-G-A

http://identifiers.org/hco/16/GRCh38#20964482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119551015-C-A

20964482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119551015-C-G

20964497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119551030-G-A

20964656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119551189-T-C

20965060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense variant
orthologous variants: 119551593-C-T

20965151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119551684-T-C

http://identifiers.org/hco/16/GRCh38#20965157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119551690-C-A

20965157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense variant
orthologous variants: 119551690-C-G

20965175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119551708-G-A

20965175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119551708-G-C

20965175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119551708-G-T

20965435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119551968-A-G

http://identifiers.org/hco/16/GRCh38#20965553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119552082-C-A

20965553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119552082-C-T

20965709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119552240-T-G

20965722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119552253-A-G

20967049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119552837-C-T

20967075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119552862-C-T

20967084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119552871-G-T

20967335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119553096-T-C

20967446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119553241-C-G

20967446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119553241-C-T

20967471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119553266-G-T

http://identifiers.org/hco/16/GRCh38#20968781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119554175-A-C

20968846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119554233-T-C

20968933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119554304-G-C

20969197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119554513-T-G

20969225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119554532-C-T

20969468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119554683-C-T

20969507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119554694-C-T

http://identifiers.org/hco/16/GRCh38#20969677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119554893-A-C

20969690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119554906-T-C

20969716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119554938-G-T

20969736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119554980-A-G

http://identifiers.org/hco/16/GRCh38#20969739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119554983-C-A

20970014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119555448-G-A

20970014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119555448-G-T

20970131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119555534-G-T

20970167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119555546-G-A

http://identifiers.org/hco/16/GRCh38#20970178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119555557-A-C

20971382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119558700-G-A

20971436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119558752-C-G

20971510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119558824-C-T

20971577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119558884-G-A

20971579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119558886-G-A

20971670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119558972-C-T

20971753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119559056-T-C

20971877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119559185-C-T

20972040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119559547-G-C

20972074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119559594-G-A

20972102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119559615-G-A

20972153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119559666-G-A

20972254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119559773-G-T

20972296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119559844-G-C

20975148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561271-G-C

20975148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561271-G-T

20975218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561343-T-C

20975221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561346-C-T

20975392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119561517-C-T

20975445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561572-G-A

http://identifiers.org/hco/16/GRCh38#20975454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119561581-C-A

20975454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561581-C-T

20975455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561582-T-A

20975505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561640-T-A

20975505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561640-T-C

20975505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561640-T-G

20975538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561673-G-T

20975709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119561843-T-C

20979223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119564598-A-T

http://identifiers.org/hco/16/GRCh38#20979243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119564614-C-A

20979543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119564898-G-A

20979543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119564898-G-T

20979648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565003-T-A

20982674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565333-C-G

20982701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565360-A-G

http://identifiers.org/hco/16/GRCh38#20982986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119565624-C-A

20982986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565624-C-T

20982989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565627-G-A

20982989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565627-G-C

20982989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565627-G-T

http://identifiers.org/hco/16/GRCh38#20983028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119565670-C-A

20983028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565670-C-T

20983445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565755-C-G

20983445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565755-C-T

20983560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565858-T-C

20983572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565870-G-A

20983622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119565912-T-C

20984932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119566514-T-C

20984980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119566561-G-A

20984980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119566561-G-C

20984980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119566561-G-T

http://identifiers.org/hco/16/GRCh38#20984990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119566571-C-A

20984990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119566571-C-T

20985146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119566728-A-G

20985167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119566749-G-A

http://identifiers.org/hco/16/GRCh38#20985206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119566788-A-C

20985416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119566998-A-G

20985416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense variant
orthologous variants: 119566998-A-T

20985718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119567300-G-A

20985748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119567330-A-G

20985749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119567331-G-C

20985756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119567338-G-A

20985756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119567338-G-C

20985756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119567338-G-T

20985792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119567370-G-A

20985792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119567370-G-T

20986669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119569479-T-C

20986706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119569515-C-G

20986985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119569778-T-C

20987011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119569804-G-A

20987113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 119570114-C-T

http://identifiers.org/hco/16/GRCh38#20987178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119570175-C-A

20987178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 119570175-C-T

20987208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 119570207-G-A

20987208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, stop_gained
orthologous variants: 119570207-G-T

20987477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570463-G-A

20987477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570463-G-T

20987527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570514-G-A

20987557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570544-G-A

20987599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570591-C-T

http://identifiers.org/hco/16/GRCh38#20987632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119570625-C-A

20987632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570625-C-T

20987638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570631-C-T

20987674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570670-T-C

http://identifiers.org/hco/16/GRCh38#20987861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119570858-A-C

20987903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570903-C-T

20987918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570918-C-G

20987918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119570918-C-T

20988073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119571072-A-G

20988112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119571104-C-G

20988112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119571104-C-T

20988131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119571121-T-A

20988131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119571121-T-C

20988179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119571167-T-A

20988237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119571210-T-A

20996282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119572979-G-T

http://identifiers.org/hco/16/GRCh38#20997024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119574032-C-A

20997024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119574032-C-T

20997032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119574041-T-G

http://identifiers.org/hco/16/GRCh38#20997068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119574073-C-A

http://identifiers.org/hco/16/GRCh38#20997085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119574089-C-A

20997085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119574089-C-T

http://identifiers.org/hco/16/GRCh38#20997097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119574101-C-A

20997097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119574101-C-T

20997111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119574115-T-C

20997249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119574254-A-G

20997255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119574260-A-G

20997356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119574362-G-A

20997504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119574508-G-A

20997504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119574508-G-T

20999299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119576626-G-T

http://identifiers.org/hco/16/GRCh38#20999401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119576728-C-A

20999541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119576867-C-G

20999601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119576874-C-T

20999809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119577019-G-C

http://identifiers.org/hco/16/GRCh38#21000201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119577348-C-A

21000234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119577381-C-G

21000234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119577381-C-T

21000438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119577585-T-C

21000663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119577807-T-A

21000663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119577807-T-C

21000744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119577881-T-C

21001212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119578747-G-A

21001406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119579063-T-C

http://identifiers.org/hco/16/GRCh38#21001482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119579349-A-C

21001505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119579368-C-T

21001548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119579402-T-A

21001626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119579479-A-G

21001671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119579530-T-A

21001671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119579530-T-C

21001759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119579600-T-C

21001921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119579744-A-T

21002277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119580074-G-C

http://identifiers.org/hco/16/GRCh38#21002320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119580105-A-C

21003050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119580485-A-G

21003289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119580702-G-C

21003289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119580702-G-T

21003332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119580744-T-C

21003333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119580745-T-G

21003334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119580746-G-T

21003421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119580818-A-G

21009109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119582574-T-C

21009212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119582680-T-C

21009353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119583019-G-A

21009464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119583117-T-A

21010411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119583601-T-A

21010663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119583748-T-C

21011100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119586243-G-T

21011114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119586252-C-T

21011159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119586287-G-A

21011885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119586755-C-T

21011965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119586867-T-C

21012034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119586937-C-T

21012438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119587346-A-G

21012530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119587434-A-T

21012569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119587474-G-A

21012615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119587499-T-C

21012615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119587499-T-G

21012688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119587565-G-T

21012727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119587604-A-G

21018929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119591707-T-A

21018938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119591716-C-T

21019005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119591785-G-T

21019134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119591935-C-T

http://identifiers.org/hco/16/GRCh38#21019539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119592013-C-A

21019552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119592027-A-G

21019593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119592067-A-G

21019597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119592071-G-A

http://identifiers.org/hco/16/GRCh38#21019973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119592420-C-A

21019973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119592420-C-T

21021928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119604836-G-A

21021928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119604836-G-T

21022019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119604919-G-A

21022019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119604919-G-C

21022168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119605045-G-T

http://identifiers.org/hco/16/GRCh38#21022180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119605056-A-C

21022193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119605069-T-A

21022193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119605069-T-C

http://identifiers.org/hco/16/GRCh38#21023411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119605528-C-A

21023411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119605528-C-T

21023413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119605530-T-C

21023445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119605560-A-G

http://identifiers.org/hco/16/GRCh38#21023606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119605764-A-C

21023829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606005-T-G

21023918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119606104-C-T

21023942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606147-A-G

21024291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606789-G-A

21024462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606944-A-G

21024504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606959-G-A

21024504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606959-G-C

21024504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606959-G-T

21024521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606976-G-T

http://identifiers.org/hco/16/GRCh38#21024527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119606982-C-A

21024527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606982-C-G

21024527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606982-C-T

21024543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606998-G-A

21024543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119606998-G-T

21024608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119607069-C-T

21024739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119607199-T-A

21027162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119608729-A-T

21027202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119608769-A-G

21027368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119608925-G-C

21027405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119608952-T-G

21030968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119610031-G-A

http://identifiers.org/hco/16/GRCh38#21031331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119610379-C-A

21031331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119610379-C-G

21031331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119610379-C-T

21031361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119610406-T-C

21031399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119610426-G-A

21031399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119610426-G-C

21031399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119610426-G-T

http://identifiers.org/hco/16/GRCh38#21031418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119610441-C-A

21031633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119610474-G-A

21031664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119610504-T-C

21033358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119615062-T-C

http://identifiers.org/hco/16/GRCh38#21033420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119615125-C-A

21033525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119615221-C-T

http://identifiers.org/hco/16/GRCh38#21033635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119615330-A-C

21033764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119615462-T-A

21033773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119615471-G-A

21033773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119615471-G-T

http://identifiers.org/hco/16/GRCh38#21033889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119615580-C-A

21033889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119615580-C-T

21033926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119615616-T-C

http://identifiers.org/hco/16/GRCh38#21033968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119615657-C-A

21034286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119615932-T-C

21034563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119616527-T-C

21034563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119616527-T-G

21034708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119617163-T-C

21035398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119617473-T-C

http://identifiers.org/hco/16/GRCh38#21035430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119617505-C-A

21035467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119617543-G-A

21035519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119617594-A-G

21035662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119617816-T-C

21035732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119617887-T-C

21035969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119618142-T-C

21036078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119618290-G-T

21036577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119618780-G-A

21036577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119618780-G-T

21036711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119618911-A-G

21036711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119618911-A-T

21036752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119618952-G-T

21036927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119619128-G-A

21036927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119619128-G-T

21037596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119619909-T-C

21037641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119619964-G-A

21037641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119619964-G-T

21037738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119620056-C-G

21037738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119620056-C-T

21037747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119620065-G-A

21038078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119620353-G-T

21038182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119620451-T-C

21038655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119621083-C-T

21039154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119621566-G-T

21039598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119621727-C-T

21039703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119621828-G-T

21039736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119621854-G-A

21039736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119621854-G-T

http://identifiers.org/hco/16/GRCh38#21039797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119621912-A-C

21039797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119621912-A-G

21039803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119621918-C-T

21039970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119622232-C-T

21039983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119622236-G-T

21040022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119622274-A-G

21040030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119622282-T-G

21040964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119622838-T-C

21041048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119622918-G-A

21041054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119622924-C-T

http://identifiers.org/hco/16/GRCh38#21042312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119628377-C-A

21042341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119628406-T-A

21042519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119628550-C-T

21049357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119628999-G-C

21049396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629035-C-T

21049508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629132-G-A

21049508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629132-G-T

21049537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629160-T-A

21049537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629160-T-C

21049549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629172-C-T

21049551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629174-G-A

21049551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629174-G-C

21049551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629174-G-T

21049554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629177-T-C

21049559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629182-G-A

21049559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629182-G-T

21049659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119629282-A-G

http://identifiers.org/hco/16/GRCh38#21049845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119629452-C-A

21049857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629467-G-C

21049857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629467-G-T

21049996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119629612-G-T

21050039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629661-C-G

21050039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629661-C-T

21050221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629761-C-T

21050332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119629888-C-T

21051070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119631173-A-T

21051326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119631483-G-C

http://identifiers.org/hco/16/GRCh38#21051345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119631520-C-A

21051349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119631524-T-C

21051355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119631530-T-C

21051453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119631627-G-T

21051522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119631686-C-T

21051618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119631798-T-C

21051665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119631843-T-A

21051678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119631856-G-A

21051705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119631883-C-T

21052729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119633296-G-A

21052816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119633389-C-T

21052823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119633396-G-A

21052823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119633396-G-C

http://identifiers.org/hco/16/GRCh38#21052840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119633413-C-A

21052862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119633435-C-T

21052871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119633444-G-A

21052894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119633467-A-G

21053525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119633786-T-C

21053609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119633870-C-G

21054068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119634286-T-A

http://identifiers.org/hco/16/GRCh38#21054283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119634438-C-A

21054329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119634481-T-G

21054391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119634542-G-A

21054391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119634542-G-C

21054391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119634542-G-T

21054505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119634653-A-G

21054562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119634706-G-T

http://identifiers.org/hco/16/GRCh38#21054609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119634759-C-A

21054609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119634759-C-G

21054655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119634803-T-C

21054990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119635106-A-G

21055509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119635469-G-C

21055671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119635623-T-C

21056176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119636495-T-G

21056279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119636598-T-C

21056465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119636678-G-T

21056466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119636679-G-A

21056515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119636728-C-T

21056953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119637718-C-T

21057111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119637867-T-C

21057317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119637912-C-T

21057415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638009-T-C

21057628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638158-G-A

21057805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638319-G-A

21057821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638334-G-A

21057898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638409-T-C

21057900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638411-G-A

21057969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638472-T-A

21057969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638472-T-G

21058065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638535-C-T

21058137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119638607-G-T

http://identifiers.org/hco/16/GRCh38#21058206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119638676-C-A

21058206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638676-C-T

21058262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638748-A-G

http://identifiers.org/hco/16/GRCh38#21058280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119638766-A-C

21058280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638766-A-T

21058367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119638912-C-T

21058462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119639039-T-C

21058537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119639123-C-T

http://identifiers.org/hco/16/GRCh38#21060132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119640060-A-C

21060151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119640079-A-G

21060178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119640106-G-A

21060178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119640106-G-C

21060178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119640106-G-T

21060230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119640157-G-C

21060230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119640157-G-T

http://identifiers.org/hco/16/GRCh38#21060491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119640421-C-A

21060491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119640421-C-G

21060491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119640421-C-T

http://identifiers.org/hco/16/GRCh38#21062187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119641023-C-A

21062239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119641071-G-A

http://identifiers.org/hco/16/GRCh38#21062383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119641213-C-A

21062383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119641213-C-T

21062422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119641243-T-A

http://identifiers.org/hco/16/GRCh38#21062463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119641286-A-C

21062497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 119641313-G-T

21062578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119641394-C-T

21062632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119641448-C-G

21062632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119641448-C-T

21062686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119641502-A-G

21062694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119641510-G-A

21062707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119641524-G-A

21062730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119641547-C-G

http://identifiers.org/hco/16/GRCh38#21062758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119641577-C-A

21062758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119641577-C-T

21062762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119641581-T-A

21062777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119641595-T-C

21062865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119641616-T-C

21062928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119641622-T-A

21062947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119641642-T-C

21062987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119641655-T-C

21062996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119641664-G-T

21063071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119641685-G-C

http://identifiers.org/hco/16/GRCh38#21063074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119641688-C-A

21063074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119641688-C-G

21063074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119641688-C-T

21063075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119641689-G-A

21063075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119641689-G-T

21063285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119641875-A-G

21063285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119641875-A-T

21063937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119642174-T-G

21064151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119642398-G-A

21064157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119642404-A-G

21064413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119642622-C-G

21064492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119642685-C-T

21064530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119642721-G-A

21064530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119642721-G-T

21064741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119642874-T-A

21064781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119642909-G-A

http://identifiers.org/hco/16/GRCh38#21064792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119642920-C-A

21065012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119643117-G-A

21065078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119643176-T-C

21066164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119644054-T-G

21067150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119644743-T-C

21067178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119644772-A-G

21067197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119644777-G-A

21067347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense variant
orthologous variants: 119644925-G-C

21067464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119645472-G-A

http://identifiers.org/hco/16/GRCh38#21067536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119645548-C-A

21067536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119645548-C-G

21067561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119645569-G-T

21067792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119645796-A-G

http://identifiers.org/hco/16/GRCh38#21067806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119645807-A-C

21067806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119645807-A-T

21067951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119645948-T-G

21068099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119646109-C-G

21068121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119646133-C-T

21068802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119646500-G-A

http://identifiers.org/hco/16/GRCh38#21068815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119646509-C-A

21069320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119646658-G-T

21069332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119646667-G-A

21069332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119646667-G-C

21069332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119646667-G-T

http://identifiers.org/hco/16/GRCh38#21069359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119646699-A-C

21069399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119646734-G-A

21069412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119646743-T-G

21069662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119646996-G-T

21069765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119647056-G-A

21070554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119648269-G-A

21070594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119648320-T-G

21070612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119648338-G-C

21070612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119648338-G-T

21070713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119648419-G-A

21070713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: stop gained
orthologous variants: 119648419-G-T

21070740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119648446-T-C

21070881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119648579-T-C

21073049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119649430-G-A

21074736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119650289-C-T

21074764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119650313-C-T

21074771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119650320-C-T

21075007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119650500-C-G

21075198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119650707-G-T

21075331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119650803-A-G

21075331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119650803-A-T

21075350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119650822-T-G

21075392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119650863-T-C

http://identifiers.org/hco/16/GRCh38#21075606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119651076-A-C

21075606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119651076-A-T

21075703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119651110-G-A

21075703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119651110-G-T

21076048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119651191-G-A

21076094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119651203-G-A

21076256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119651355-G-A

21076446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119651530-G-C

21080465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119652617-T-A

21080478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119652635-T-C

21080587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119652731-G-A

21080658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119652808-G-A

21080658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119652808-G-T

21080662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119652812-G-A

21080790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119652975-G-A

21081236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653516-T-C

21081269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653550-G-C

21081320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653593-G-A

http://identifiers.org/hco/16/GRCh38#21081349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119653622-A-C

21081367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653640-G-A

http://identifiers.org/hco/16/GRCh38#21081481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119653720-C-A

21081481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653720-C-T

21081484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653723-G-A

21081484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653723-G-T

21081671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119653861-A-G

21081747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653938-G-C

21081747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653938-G-T

http://identifiers.org/hco/16/GRCh38#21081749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119653940-A-C

21081768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653959-C-T

21081794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653984-G-T

21081797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653987-G-C

21081797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653987-G-T

21081805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653995-T-A

21081805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119653995-T-C

21081813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119654001-T-A

21081813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119654001-T-C

21081829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119654017-G-A

21081829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119654017-G-T

http://identifiers.org/hco/16/GRCh38#21081848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119654037-C-A

21081848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119654037-C-G

21081853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119654042-G-T

http://identifiers.org/hco/16/GRCh38#21081865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119654054-C-A

21081865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119654054-C-G

21081865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119654054-C-T

http://identifiers.org/hco/16/GRCh38#21082918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119656222-C-A

http://identifiers.org/hco/16/GRCh38#21085720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119657560-C-A

21085729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119657569-C-T

21085784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119657653-C-T

http://identifiers.org/hco/16/GRCh38#21086600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119658156-C-A

http://identifiers.org/hco/16/GRCh38#21086780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119658341-C-A

21086780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658341-C-T

http://identifiers.org/hco/16/GRCh38#21086807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119658370-C-A

21086807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658370-C-T

21086813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658376-T-C

21086829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658388-G-A

21086891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119658444-A-G

21086975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: synonymous variant
orthologous variants: 119658528-C-T

21087029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 119658582-A-G

21087076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658625-G-A

21087076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658625-G-T

21087085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658634-G-C

21087085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658634-G-T

http://identifiers.org/hco/16/GRCh38#21087118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119658662-C-A

21087144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658689-T-C

21087195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658745-A-G

21087248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658780-C-G

21087329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119658863-G-A

21087999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119659429-A-G

21097004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119659771-C-G

http://identifiers.org/hco/16/GRCh38#21097046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119659807-C-A

21097046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119659807-C-T

21097198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119659966-C-T

21097246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660015-T-C

21097289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660035-A-G

21097313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660059-C-G

21097313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660059-C-T

21097320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660066-C-T

21097347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 119660097-C-T

21097371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 119660121-T-C

21097528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660278-G-T

21097535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660285-G-A

21097535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660285-G-C

21097535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660285-G-T

http://identifiers.org/hco/16/GRCh38#21097547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119660297-A-C

21097547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660297-A-T

21097582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660332-C-T

http://identifiers.org/hco/16/GRCh38#21097590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119660340-C-A

21097590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660340-C-G

21097590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660340-C-T

21097756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660461-T-C

21098032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660749-A-G

http://identifiers.org/hco/16/GRCh38#21098603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119660972-C-A

21098603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119660972-C-G

21099050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661358-C-T

21099053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661362-A-G

21099268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661564-G-A

21099276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661572-A-G

http://identifiers.org/hco/16/GRCh38#21099298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119661594-A-C

21099309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661605-G-C

21099374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661675-T-C

21099502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661791-C-T

21099547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661834-G-C

21099613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661896-A-G

21099613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661896-A-T

21099685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661966-C-G

21099735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119661997-T-C

21099981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119662168-C-G

21099981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119662168-C-T

21100030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119662212-T-G

http://identifiers.org/hco/16/GRCh38#21100366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119665742-C-A

21100509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119665879-T-G

21100610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119665969-A-G

21100632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, undefined
orthologous variants: 119665990-T-A

21100632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, undefined
orthologous variants: 119665990-T-C

21100762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119666084-C-T

21100769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119666091-A-T

21100777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119666099-T-C

21100788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119666109-T-C

21100794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119666115-C-T

21100883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119666197-A-G

http://identifiers.org/hco/16/GRCh38#21100979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119666291-A-C

21101800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119667125-C-T

21101813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119667138-C-T

21101874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119667209-C-T

21102128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119667428-G-A

21102128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119667428-G-C

21102159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119667457-T-C

21102396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119667794-T-C

21103907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668309-G-A

21103907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668309-G-T

http://identifiers.org/hco/16/GRCh38#21103967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119668369-C-A

21103967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668369-C-T

21104073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668470-A-G

21104148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668562-G-A

21104148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668562-G-C

21104148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668562-G-T

http://identifiers.org/hco/16/GRCh38#21104194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119668608-C-A

21104214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668627-C-G

21104244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668652-G-T

http://identifiers.org/hco/16/GRCh38#21104284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119668681-C-A

21104284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668681-C-G

21104284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119668681-C-T

http://identifiers.org/hco/16/GRCh38#21104338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119668717-C-A

21104657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119669020-G-A

21104657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119669020-G-T

21104681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119669043-T-C

21104701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119669068-G-A

21104701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119669068-G-T

21104745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119669123-A-G

21104957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119669318-T-C

21104993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119669354-C-T

21105144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119669466-G-A

21106313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119669981-G-T

21106340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119670009-T-C

21106348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119670017-G-A

21106348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119670017-G-T

http://identifiers.org/hco/16/GRCh38#21106360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119670029-C-A

21106360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119670029-C-T

http://identifiers.org/hco/16/GRCh38#21106371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119670040-C-A

21106371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119670040-C-T

21106450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119670099-A-G

21106484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119670128-A-G

http://identifiers.org/hco/16/GRCh38#21106494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119670138-C-A

21106494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119670138-C-T

21106512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119670156-C-T

21106560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119670204-G-C

21106560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119670204-G-T

21106590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119670234-G-T

21106602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119670246-G-A

21106602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119670246-G-T

21111642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 119670716-G-A

http://identifiers.org/hco/16/GRCh38#21111802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119670876-C-A

21111802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 119670876-C-T

21111879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119670953-C-T

21111923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119670994-C-T

21111979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119671050-G-A

http://identifiers.org/hco/16/GRCh38#21111984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119671055-A-C

http://identifiers.org/hco/16/GRCh38#21112103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119671174-C-A

21112103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119671174-C-T

21112127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119671198-C-T

21112184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119671254-A-G

21112184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119671254-A-T

21112185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119671255-G-T

http://identifiers.org/hco/16/GRCh38#21116852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119672452-A-C

21117008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119672569-A-G

21117128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119672695-T-C

21117139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119672706-G-C

21117139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119672706-G-T

21117177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119672746-G-A

21117177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119672746-G-T

21117256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119672814-A-T

21117370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119672933-C-G

21117370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119672933-C-T

21117373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119672937-G-A

21117373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119672937-G-T

21117377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119672941-T-A

21117377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119672941-T-G

21117419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119672980-C-T

21117467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119673030-G-A

21117467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119673030-G-T

21117588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119673156-C-G

21118817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119674399-C-T

21118839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119674421-A-G

21118915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119674500-G-C

21118915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119674500-G-T

21118961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119674546-T-C

21118962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119674547-G-A

21120519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119675436-T-C

21120525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119675441-A-T

21120574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119675486-G-A

21120574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119675486-G-T

21120707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119675631-G-A

21120719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119675643-A-G

21120724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119675648-G-T

http://identifiers.org/hco/16/GRCh38#21120779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/7/GRCm39#119675717-C-A

21120779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119675717-C-T

http://identifiers.org/hco/16/GRCh38#21120804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119675742-C-A

21120867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119675804-A-G

http://identifiers.org/hco/16/GRCh38#21120908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119675843-C-A

21120912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119675847-G-A

21120912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119675847-G-T

http://identifiers.org/hco/16/GRCh38#21120935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119675870-C-A

http://identifiers.org/hco/16/GRCh38#21120963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119675895-C-A

21121106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119676408-G-A

21121106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119676408-G-C

21121106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119676408-G-T

21121158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119676460-C-T

http://identifiers.org/hco/16/GRCh38#21121195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119676497-C-A

21121804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119676859-G-T

21121956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119677011-C-T

21121988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119677043-T-A

21125271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 119677696-T-C

21125338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119677763-G-A

21126461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119678152-A-G

21127629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119678534-A-T

21127705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119678599-T-C

21127822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119678716-G-C

21127826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119678720-G-A

21127826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119678720-G-T

21132460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119679963-A-G

21132501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119680001-T-C

21132508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119680009-A-G

21132554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119680055-G-A

21132594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119680089-T-C

21132607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119680102-T-C

21133992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119682072-C-T

21134073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119682153-G-T

21134080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119682160-A-G

21134082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119682161-G-A

21134082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119682161-G-T

21134191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119682257-G-A

21134191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119682257-G-T

21134197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119682263-G-C

http://identifiers.org/hco/16/GRCh38#21134206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119682272-C-A

21134206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119682272-C-T

21134232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119682297-T-A

21134503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119682572-G-A

21134503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119682572-G-T

http://identifiers.org/hco/16/GRCh38#21136276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119684279-C-A

21136276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684279-C-T

http://identifiers.org/hco/16/GRCh38#21136291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119684294-C-A

21136397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119684395-G-T

21136483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119684481-G-A

21136483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119684481-G-C

21136483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119684481-G-T

21136490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119684488-A-G

21136524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119684522-C-T

21136552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119684544-T-C

21136561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119684553-G-T

21136596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684597-C-T

21136651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684634-G-A

21136651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684634-G-T

21136671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684654-T-C

21136671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684654-T-G

21136788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684745-G-A

21136868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684861-C-T

21136916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684915-C-T

21136930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684944-C-T

21136959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684973-C-G

21136959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119684973-C-T

http://identifiers.org/hco/16/GRCh38#21140248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119685144-C-A

21140260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119685152-G-A

21140260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119685152-G-T

21140329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119685233-G-T

http://identifiers.org/hco/16/GRCh38#21140364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119685240-C-A

21140364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119685240-C-T

21140385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119685265-G-A

21140420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119685291-T-G

http://identifiers.org/hco/16/GRCh38#21140451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119685322-C-A

http://identifiers.org/hco/16/GRCh38#21140481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119685346-A-C

21140497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119685360-C-T

21140638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119685501-T-C

21140653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119685516-T-C

http://identifiers.org/hco/16/GRCh38#21140749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119685606-C-A

21140789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119685650-T-A

21140789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119685650-T-G

http://identifiers.org/hco/16/GRCh38#21140821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119685673-C-A

21140821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119685673-C-T

21141192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119685823-A-T

21141272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119685906-T-C

http://identifiers.org/hco/16/GRCh38#21141276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119685910-C-A

21141276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119685910-C-T

21141277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119685911-T-A

21141277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119685911-T-C

21141302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 119685936-A-G

21141341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119685975-T-A

21141341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119685975-T-C

21141341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119685975-T-G

21141413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119686054-G-A

21141413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119686054-G-T

http://identifiers.org/hco/16/GRCh38#21141459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119686101-C-A

21141459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119686101-C-T

21141481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119686123-G-A

21141481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119686123-G-C

21141481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119686123-G-T

21141501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119686143-T-A

21141585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119686209-C-T

21145141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689042-A-G

21145167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689071-A-G

21145169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689073-T-C

21145169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689073-T-G

21145197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119689098-C-T

21145275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119689176-G-A

21145420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689319-A-G

http://identifiers.org/hco/16/GRCh38#21145466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119689357-C-A

21145466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689357-C-G

21145466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689357-C-T

21145525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689390-T-A

21145525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689390-T-C

http://identifiers.org/hco/16/GRCh38#21145527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119689392-C-A

21145527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689392-C-T

21145542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689407-G-T

21145614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689468-C-T

http://identifiers.org/hco/16/GRCh38#21145847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119689671-C-A

http://identifiers.org/hco/16/GRCh38#21145862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119689686-C-A

21145862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689686-C-T

21145881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689705-G-A

21145881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689705-G-T

21145906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689721-G-A

21145906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689721-G-T

21145920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689735-G-A

21145920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689735-G-T

21145944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689759-C-T

21145972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689787-A-G

21146062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119689877-G-A

21146102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689916-G-A

21146102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689916-G-T

21146154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119689968-T-C

21146193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119690004-G-A

21147135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119690129-C-T

21147154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119690148-T-C

21147558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 119690538-C-T

21147635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119690613-A-G

21147717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119690662-G-A

21147817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119690754-T-G

21147980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119690900-T-G

21147989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119690911-A-G

21148115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119691032-G-A

21148147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119691067-T-C

21148925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119693251-T-G

21149299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119693299-A-G

21150261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119694342-A-G

21150307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119694388-C-T

21150364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119694442-G-A

http://identifiers.org/hco/16/GRCh38#21150446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119694521-C-A

21150446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119694521-C-T

21150473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119694547-G-A

21150473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119694547-G-C

21150630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119694691-G-A

21150698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119694766-G-C

21150749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 119694815-A-G

21150754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119694820-T-A

21150754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119694820-T-C

21150754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 119694820-T-G

21150884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119694947-G-A

21150884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119694947-G-T

21150960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695009-G-T

21150987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695036-G-T

21150991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695040-G-A

http://identifiers.org/hco/16/GRCh38#21151002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119695048-A-C

21151061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695102-C-T

21151269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695243-G-C

21151324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695267-T-G

21151369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695313-G-A

21151584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695518-T-C

21151602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695588-T-C

21151624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695611-T-C

21151637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695624-C-T

21151801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695791-C-T

21151847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119695838-T-G

21156813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, undefined
orthologous variants: 119697173-A-G

http://identifiers.org/hco/16/GRCh38#21156858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119697203-A-C

21156913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, undefined
orthologous variants: 119697255-A-G

21156929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, undefined
orthologous variants: 119697268-C-T

http://identifiers.org/hco/16/GRCh38#21157025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119697315-A-C

21157125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119697414-G-A

21157239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119697520-T-C

21157735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119700598-G-A

http://identifiers.org/hco/16/GRCh38#21157871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119700796-C-A

21157947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119700861-A-G

21157982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119700897-A-G

21157983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119700898-A-G

21158033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119700964-T-G

21158042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119700973-A-G

21158114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron variant
orthologous variants: 119701026-C-T

21158206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, undefined
orthologous variants: 119701127-G-T

21158273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, undefined
orthologous variants: 119701196-G-A

21158273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, undefined
orthologous variants: 119701196-G-T

21158399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119701289-T-C

21158400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119701290-T-C

http://identifiers.org/hco/16/GRCh38#21158417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119701307-C-A

21158417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119701307-C-T

21158454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119701344-C-T

21158456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119701346-G-T

http://identifiers.org/hco/16/GRCh38#21158461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119701351-C-A

http://identifiers.org/hco/16/GRCh38#21158565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119701475-C-A

21158565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119701475-C-T

21158587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119701532-A-G

21158627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119701570-G-A

21158627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 119701570-G-T

21158679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119701670-G-A

21158679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119701670-G-T

http://identifiers.org/hco/16/GRCh38#21158717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119701708-C-A

21158717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 119701708-C-T

21158775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119701763-T-G

21159154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119702108-A-G

http://identifiers.org/hco/16/GRCh38#21159237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119702190-C-A

21159237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119702190-C-T

21159288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119702241-G-A

21159288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119702241-G-C

21159288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119702241-G-T

http://identifiers.org/hco/16/GRCh38#21159342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119702293-C-A

21159342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119702293-C-G

21159342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119702293-C-T

21159352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 119702298-T-C

21159352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119702298-T-G

http://identifiers.org/hco/16/GRCh38#21159366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119702310-C-A

21159366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119702310-C-T

21159367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 119702311-T-C

http://identifiers.org/hco/16/GRCh38#21159425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119702368-C-A

21159425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2949
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 119702368-C-T