Gene >> GPT2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340124 |
| Start |
46927030:46927030(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1474C>T |
| AA Mutation |
p.His492Tyr(p.H492Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340124 |
| Start |
46922297:46922297(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1093G>T |
| AA Mutation |
p.Gly365Cys(p.G365C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |