Gene >> ETV6
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000396373 |
| Start |
11884472:11884472(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1037A>G |
| AA Mutation |
p.Tyr346Cys(p.Y346C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000396373 |
| Start |
11869845:11869845(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs140005721
|
| CDS Mutation |
c.885C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |