Gene >> RNF135
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000328381 |
| Start |
30998914:30998914(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1022G>T |
| AA Mutation |
p.Gly341Val(p.G341V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000328381 |
| Start |
30998698:30998698(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.806C>T |
| AA Mutation |
p.Ser269Phe(p.S269F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |