Gene >> BRCA2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380152 |
| Start |
32338895:32338895(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.4540G>C |
| AA Mutation |
p.Glu1514Gln(p.E1514Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380152 |
| Start |
32337731:32337731(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3376G>A |
| AA Mutation |
p.Glu1126Lys(p.E1126K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |