Gene >> RRM1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000300738 |
| Start |
4107524:4107524(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.376G>A |
| AA Mutation |
p.Ala126Thr(p.A126T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000300738 |
| Start |
4121604:4121604(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.877C>T |
| AA Mutation |
p.Arg293Cys(p.R293C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |