Gene >> PGC
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373025 |
| Start |
41736908:41736908(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1111T>C |
| AA Mutation |
p.Tyr371His(p.Y371H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373025 |
| Start |
41744403:41744403(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770437031
|
| CDS Mutation |
c.322G>A |
| AA Mutation |
p.Ala108Thr(p.A108T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |