Gene >> RNF13
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344229 |
| Start |
149872105:149872105(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.272G>A |
| AA Mutation |
p.Gly91Asp(p.G91D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000344229 |
| Start |
149852554:149852554(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.153C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |