Gene >> PTGS1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000362012 |
| Start |
122392473:122392473(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs533328230
|
| CDS Mutation |
c.1729G>A |
| AA Mutation |
p.Val577Ile(p.V577I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000362012 |
| Start |
122381537:122381537(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.663G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |