Gene >> PRG2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311862 |
| Start |
57387774:57387774(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.590G>A |
| AA Mutation |
p.Cys197Tyr(p.C197Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311862 |
| Start |
57389928:57389928(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.17T>G |
| AA Mutation |
p.Leu6Arg(p.L6R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |