Gene >> P2RY12
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302632 |
| Start |
151338279:151338279(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.567A>G |
| AA Mutation |
p.Ile189Met(p.I189M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000302632 |
| Start |
151337975:151337975(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.871G>T |
| AA Mutation |
p.Ala291Ser(p.A291S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |