Gene >> ETV5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306376 |
| Start |
186057082:186057082(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1202C>T |
| AA Mutation |
p.Pro401Leu(p.P401L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306376 |
| Start |
186065897:186065897(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.826C>G |
| AA Mutation |
p.Pro276Ala(p.P276A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |