Gene >> PHB
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000300408 |
| Start |
49405164:49405164(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.647G>A |
| AA Mutation |
p.Gly216Asp(p.G216D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000300408 |
| Start |
49409435:49409435(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.289C>T |
| AA Mutation |
p.Arg97Trp(p.R97W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |