Gene >> AKT2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000392038 |
| Start |
40236264:40236264(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.953C>T |
| AA Mutation |
p.Ala318Val(p.A318V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000392038 |
| Start |
40255250:40255250(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755782228
|
| CDS Mutation |
c.195C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |