Gene >> ETV5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306376 |
| Start |
186048701:186048701(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs773704999
|
| CDS Mutation |
c.1471G>A |
| AA Mutation |
p.Ala491Thr(p.A491T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000306376 |
| Start |
186105863:186105863(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200588942
|
| CDS Mutation |
c.6C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |