Gene >> PTGDR
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306051 |
| Start |
52274749:52274749(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.865G>T |
| AA Mutation |
p.Ala289Ser(p.A289S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000306051 |
| Start |
52268522:52268522(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.708G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |