Gene >> PVR
| ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000425690 |
| Start |
44661741:44661741(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1184A>T |
| AA Mutation |
p.His395Leu(p.H395L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000425690 |
| Start |
44658877:44658877(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1127G>T |
| AA Mutation |
p.Trp376Leu(p.W376L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |