Gene >> PTGER2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000245457 |
| Start |
52315012:52315012(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.464C>A |
| AA Mutation |
p.Ala155Asp(p.A155D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000245457 |
| Start |
52314960:52314960(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.412A>G |
| AA Mutation |
p.Ile138Val(p.I138V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |