Gene >> FATE1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370350 |
| Start |
151716196:151716196(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.77G>C |
| AA Mutation |
p.Gly26Ala(p.G26A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000370350 |
| Start |
151716124:151716124(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.5C>A |
| AA Mutation |
p.Ala2Glu(p.A2E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |