Gene >> E2F1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000343380 |
| Start |
33676873:33676873(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1173C>G |
| AA Mutation |
p.Phe391Leu(p.F391L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000343380 |
| Start |
33676750:33676750(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752347181
|
| CDS Mutation |
c.1296C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |