Gene >> RCVRN
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226193 |
| Start |
9904805:9904805(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.376G>A |
| AA Mutation |
p.Val126Ile(p.V126I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000226193 |
| Start |
9904985:9904985(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.196G>A |
| AA Mutation |
p.Ala66Thr(p.A66T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |