Gene >> PAG1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220597 |
| Start |
80976741:80976741(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1102A>C |
| AA Mutation |
p.Thr368Pro(p.T368P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220597 |
| Start |
80976899:80976899(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.944C>A |
| AA Mutation |
p.Ala315Asp(p.A315D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |