Gene >> F2R
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000319211 |
| Start |
76732598:76732598(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.373G>A |
| AA Mutation |
p.Val125Ile(p.V125I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000319211 |
| Start |
76732326:76732326(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.101C>T |
| AA Mutation |
p.Thr34Ile(p.T34I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |