Gene >> BRAF
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000288602 |
| Start |
140801416:140801416(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.856C>G |
| AA Mutation |
p.Leu286Val(p.L286V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000288602 |
| Start |
140801550:140801550(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs387906660
|
| CDS Mutation |
c.722C>T |
| AA Mutation |
p.Thr241Met(p.T241M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |