Gene >> E2F3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000346618 |
| Start |
20402278:20402278(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.46G>A |
| AA Mutation |
p.Ala16Thr(p.A16T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000346618 |
| Start |
20490386:20490386(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1354G>A |
| AA Mutation |
p.Asp452Asn(p.D452N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |