Gene >> PGC
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373025 |
| Start |
41744750:41744750(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.118G>A |
| AA Mutation |
p.Gly40Arg(p.G40R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373025 |
| Start |
41742378:41742378(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.559C>G |
| AA Mutation |
p.Leu187Val(p.L187V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |