113977906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13617336-A-T

113978149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13617544-G-T

113978191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13617582-A-G

113978623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13617979-C-T

http://identifiers.org/hco/13/GRCh38#113978641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13617997-C-A

http://identifiers.org/hco/13/GRCh38#113978776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13618118-C-A

113978776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618118-C-G

113978776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618118-C-T

http://identifiers.org/hco/13/GRCh38#113978780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13618122-C-A

113978780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618122-C-T

113978817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618158-G-A

113978817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618158-G-T

113978850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618197-T-C

http://identifiers.org/hco/13/GRCh38#113978904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13618252-C-A

113978904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618252-C-T

113978908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618256-G-A

113978908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618256-G-T

113978997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618319-T-C

113978997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618319-T-G

113979082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618410-G-A

113979082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618410-G-T

http://identifiers.org/hco/13/GRCh38#113979198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13618531-A-C

113979198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618531-A-G

113979198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618531-A-T

http://identifiers.org/hco/13/GRCh38#113979239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13618583-C-A

113979239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618583-C-T

113979285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618644-T-C

113979317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618667-G-T

113979335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618680-G-A

113979335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 3 prime UTR variant
orthologous variants: 13618680-G-T

113979447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13618792-A-G

113979462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13618807-C-G

113979462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13618807-C-T

113979497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13618863-T-C

http://identifiers.org/hco/13/GRCh38#113979522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13618888-C-A

113979614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13618985-G-A

113979663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13619029-T-C

113979700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13619107-A-T

113979712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13619119-G-A

http://identifiers.org/hco/13/GRCh38#113981611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13620176-C-A

113981611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620176-C-G

113981611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620176-C-T

113981623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620187-T-A

113981623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620187-T-C

http://identifiers.org/hco/13/GRCh38#113981637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13620201-C-A

113981689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13620253-C-T

113981752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13620316-G-A

113981800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13620364-G-A

113981800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: missense variant
orthologous variants: 13620364-G-C

113981812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: missense variant
orthologous variants: 13620376-C-G

113981812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13620376-C-T

113981836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13620400-C-T

113981870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620443-G-A

113981927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620503-G-A

113981927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620503-G-T

http://identifiers.org/hco/13/GRCh38#113981977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13620522-C-A

113981977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620522-C-T

113981979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620524-G-A

113981979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620524-G-C

113981979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620524-G-T

http://identifiers.org/hco/13/GRCh38#113982070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13620595-C-A

113982235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620753-T-G

113982400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13620893-G-C

113982526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13621007-C-G

113982526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13621007-C-T

113982568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13621047-C-G

113982904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13621766-C-T

113983237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13622033-T-C

113983463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13622249-G-A

113983463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13622249-G-C

113983463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13622249-G-T

113983623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13622354-G-A

113983702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13622433-A-G

113983854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13622581-G-A

113983857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13622584-G-A

http://identifiers.org/hco/13/GRCh38#113992235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13626110-A-C

113992302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13626175-C-T

113992307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13626180-T-C

http://identifiers.org/hco/13/GRCh38#113992363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13626236-C-A

113992363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13626236-C-T

http://identifiers.org/hco/13/GRCh38#113992410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13626263-C-A

113992410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13626263-C-G

113992410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13626263-C-T

113992432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13626288-G-T

http://identifiers.org/hco/13/GRCh38#113992447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13626303-C-A

113996432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13627252-T-C

113996480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13627293-G-A

113996480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13627293-G-T

http://identifiers.org/hco/13/GRCh38#113996485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13627298-C-A

113996485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13627298-C-G

113996485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13627298-C-T

113996516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13627345-G-A

113996516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13627345-G-C

113996516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13627345-G-T

113996608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13627437-C-T

113996656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13627485-G-A

113999609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13627831-C-T

114000953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13628736-G-A

114000953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13628736-G-C

114000953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13628736-G-T

http://identifiers.org/hco/13/GRCh38#114001004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13628795-C-A

114001004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13628795-C-T

114001028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13628819-G-T

114007604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 13630105-G-T

114007612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 13630113-G-T

114007649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630149-T-A

114007649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630149-T-C

114007727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630219-T-A

114007727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630219-T-G

114007730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630222-G-A

114007730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630222-G-C

114007730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630222-G-T

114007748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630237-G-A

114007748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630237-G-T

114007752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630241-G-A

114007752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13630241-G-T

http://identifiers.org/hco/13/GRCh38#114009368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13631237-A-C

114009368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13631237-A-G

114009476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13631340-C-T

114009488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13631350-G-A

114009488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13631350-G-C

114009488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13631350-G-T

114011146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13632274-G-A

114011146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13632274-G-T

114011246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 13632374-G-A

114011246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 13632374-G-C

114011246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 13632374-G-T

114013159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: missense variant
orthologous variants: 13633767-G-A

114013226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13633834-A-G

114013288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13633889-A-G

114013299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13633903-G-A

114013299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13633903-G-T

http://identifiers.org/hco/13/GRCh38#114013326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13633923-A-C

114013326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13633923-A-G

114013340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13633935-A-G

114013440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13634028-T-C

114013484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13634066-T-A

114015239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: missense_variant, undefined
orthologous variants: 13634943-G-T

114015327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: missense variant
orthologous variants: 13635031-G-T

http://identifiers.org/hco/13/GRCh38#114015365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13635062-C-A

114015365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635062-C-G

114015365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635062-C-T

http://identifiers.org/hco/13/GRCh38#114015439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#13635108-C-A

114015439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13635108-C-T

114015475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13635140-G-A

114015475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13635140-G-T

http://identifiers.org/hco/13/GRCh38#114015476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#13635141-C-A

114015476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13635141-C-T

114015572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635205-G-A

114015572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635205-G-T

114015743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635345-A-G

114015804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635382-A-T

114015844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635400-C-T

114015868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635411-T-C

114016061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635541-G-A

http://identifiers.org/hco/13/GRCh38#114016070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13635550-A-C

114016070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635550-A-T

http://identifiers.org/hco/13/GRCh38#114016072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13635552-C-A

114016072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635552-C-T

http://identifiers.org/hco/13/GRCh38#114016085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13635563-C-A

114016085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635563-C-T

114016103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635581-G-A

114016103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635581-G-C

114016129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635600-C-T

http://identifiers.org/hco/13/GRCh38#114016133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13635604-C-A

114016133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635604-C-T

114016159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635627-A-T

http://identifiers.org/hco/13/GRCh38#114016181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13635649-C-A

114016181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635649-C-T

114016209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13635686-A-G

http://identifiers.org/hco/13/GRCh38#114016320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13635781-A-C

114016320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635781-A-G

114016322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635783-G-A

114016322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635783-G-T

114016339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635803-G-C

114016339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635803-G-T

114016344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635808-C-T

114016368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635817-T-A

114016368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635817-T-C

114016368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635817-T-G

http://identifiers.org/hco/13/GRCh38#114016397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13635847-C-A

114016397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635847-C-T

114016470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635953-T-C

114016474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13635957-G-A

114016531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13636011-G-A

114017282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13636919-C-G

114017282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: synonymous variant
orthologous variants: 13636919-C-T

114017395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13637031-G-A

114017395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13637031-G-T

114018095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13637943-G-T

114018238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 13638086-A-G

114018238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 13638086-A-T

114018310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638240-G-A

114018310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638240-G-T

http://identifiers.org/hco/13/GRCh38#114018316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13638256-A-C

114018316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638256-A-G

114018459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638554-G-A

114018469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638564-T-C

114018545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638647-C-T

114018618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638744-G-A

114018618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638744-G-C

114018618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638744-G-T

114018666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638790-G-C

114018666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638790-G-T

114018703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638830-G-A

114018754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638855-G-A

114018754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638855-G-C

114018754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638855-G-T

114018760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13638861-C-T

114018772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 13638873-C-G

114018772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 13638873-C-T

114018826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 13638927-G-A

114018895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 13638996-A-T

114018943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13639036-G-A

114018943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13639036-G-C

114018947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13639040-G-A

114018981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13639067-A-G

114021314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13640143-A-G

114021429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13640227-G-A

114021445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13640243-G-A

114021445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13640243-G-T

114021493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13640291-A-G

114027038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13645101-G-A

114027407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13645353-A-G

114027482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13645428-A-G

http://identifiers.org/hco/13/GRCh38#114027542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13645493-A-C

http://identifiers.org/hco/13/GRCh38#114027545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13645496-C-A

114027545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13645496-C-T

114027600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13645547-T-A

114027600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13645547-T-C

114027693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13645640-G-A

114027693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13645640-G-T

114027714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13645658-A-G

114027802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13645753-G-T

114029819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13648222-G-A

114029819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13648222-G-C

114029819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13648222-G-T

114036270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13652314-A-G

114039632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13654989-C-T

114039661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13655017-C-T

http://identifiers.org/hco/13/GRCh38#114039682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13655038-C-A

114040993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 13655855-G-A

114041015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 13655877-A-G

114041018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 13655880-G-A

114041097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 13655959-G-A

114044537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13656502-C-T

114044615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13656577-A-G

114044764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13656736-A-G

114044854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13656827-T-A

http://identifiers.org/hco/13/GRCh38#114050939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13660429-C-A

114050939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13660429-C-T

114053171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13664931-G-A

114053180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13664940-C-T

114053243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13665003-G-C

114053468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13665272-C-T

114053775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13665582-T-C

114064883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 13673666-G-A

114064884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 13673667-G-A

114064900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 13673683-C-G

114066717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13675788-G-T

114071641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13680521-A-G

114071788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13680648-G-A

114072308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13681073-G-A

114072387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13681152-G-C

114073728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 13681783-C-G

114114279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13714404-C-G

114114289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13714414-C-G

114114326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13714447-G-A

http://identifiers.org/hco/13/GRCh38#114119066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13718261-C-A

114119189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13718375-C-T

114119311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13718498-C-T

114121201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719191-C-T

114121213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719204-G-A

114121274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719222-G-A

114121402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719344-T-C

114121403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719345-T-C

114121662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719600-T-A

114121728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719645-G-C

114121732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719649-C-T

114121740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719657-G-A

114121863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719766-G-A

114121863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719766-G-T

114121908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719791-T-C

114121973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719863-G-A

114122113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13719967-G-A

114122280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: 13720123-C-T

http://identifiers.org/hco/13/GRCh38#114122317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13720160-A-C

114128053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13723047-C-T

114128112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13723106-G-A

http://identifiers.org/hco/13/GRCh38#114128231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13723236-C-A

114128231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13723236-C-T

114128568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13723562-G-A

114128872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 13724158-G-A

114128875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13724161-G-A

114128889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13724193-G-A

114129433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 13724737-G-C

114129503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13724780-G-T

114129877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13725170-A-G

114130268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 13725721-G-A

114130286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13725739-G-A

114130337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13725758-C-T

114130628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13725921-T-C

114130641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13725933-C-T

114130731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13726032-C-T

114130776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13726080-T-C

114131368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13726631-G-A

http://identifiers.org/hco/13/GRCh38#114131583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13726846-C-A

114131954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13727031-G-C

114132093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13727166-A-G

114132419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13727382-G-A

114132419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13727382-G-C

114132419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: intron_variant, undefined
orthologous variants: 13727382-G-T

http://identifiers.org/hco/13/GRCh38#114132537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#13727501-C-A

114132537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5 prime UTR variant
orthologous variants: 13727501-C-G

114132537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5 prime UTR variant
orthologous variants: 13727501-C-T

114132575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5 prime UTR variant
orthologous variants: 13727555-G-A

114132575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20331
most severe consequence: 5 prime UTR variant
orthologous variants: 13727555-G-C