COSMIC:
COSM4658355 (not active)
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00840469 (NFE)
Genomes Max Group AF
0.00749785 (NFE)
Exomes Max Group AF
0.00842986 (NFE)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16165722G>A , CM000678.2:g.16165722G>A | GRCh38 |
| NC_000016.9:g.16259579G>A , CM000678.1:g.16259579G>A | GRCh37 |
| NC_000016.8:g.16167080G>A | NCBI36 |
| NG_007558.2:g.62750C>T | |
| NG_007558.3:g.62896C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622290.5:c.3207C>T | ENSP00000483331.2:p.Tyr1069= | |
| ENST00000205557.12:c.3207C>T MANE Select | ENSP00000205557.7:p.Tyr1069= | |
| ENST00000640696.1:c.222C>T | ENSP00000492197.1:p.Tyr74= | |
| ENST00000205557.11:c.3207C>T | ENSP00000205557.7:p.Tyr1069= | |
| ENST00000456970.6:c.3032C>T | ENSP00000405002.2:n.3032C>T | |
| ENST00000622290.4:c.*416C>T | ENSP00000483331.1:n.*416C>T | |
| NM_001171.5:c.3207C>T | NP_001162.4:p.Tyr1069= | |
| XM_011522479.1:c.3174C>T | XP_011520781.1:p.Tyr1058= | |
| XM_011522480.1:c.2865C>T | XP_011520782.1:p.Tyr955= | |
| XM_011522481.1:c.2865C>T | XP_011520783.1:p.Tyr955= | |
| XR_932836.1:n.3442C>T | ||
| XR_932837.1:n.3443C>T | ||
| XR_932838.1:n.3443C>T | ||
| NM_001351800.1:c.2865C>T | NP_001338729.1:p.Tyr955= | |
| NR_147784.1:n.3069C>T | ||
| XM_011522479.2:c.3174C>T | XP_011520781.1:p.Tyr1058= | |
| XM_011522481.3:c.2865C>T | XP_011520783.1:p.Tyr955= | |
| XM_017023212.1:c.3039C>T | XP_016878701.1:p.Tyr1013= | |
| XM_017023214.1:c.3207C>T | XP_016878703.1:p.Tyr1069= | |
| XM_024450261.1:c.3243C>T | XP_024306029.1:p.Tyr1081= | |
| XR_932836.2:n.3388C>T | ||
| XR_932837.3:n.3388C>T | ||
| XR_932838.3:n.3388C>T | ||
| NM_001171.6:c.3207C>T MANE Select | NP_001162.5:p.Tyr1069= |