Gene >> GP2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000381362 |
| Start |
20318269:20318269(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145287300
|
| CDS Mutation |
c.1178G>A |
| AA Mutation |
p.Arg393Gln(p.R393Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000381362 |
| Start |
20319725:20319725(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.911T>C |
| AA Mutation |
p.Val304Ala(p.V304A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |