Gene >> PTGDR
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306051 |
| Start |
52268442:52268442(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.628C>A |
| AA Mutation |
p.Leu210Met(p.L210M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000306051 |
| Start |
52268613:52268613(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.799C>A |
| AA Mutation |
p.Leu267Met(p.L267M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |