Gene >> FGF1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000337706 |
| Start |
142595426:142595426(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.332C>T |
| AA Mutation |
p.Thr111Ile(p.T111I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000337706 |
| Start |
142595424:142595424(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.334T>C |
| AA Mutation |
p.Tyr112His(p.Y112H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |