Gene >> STK38L
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000389032 |
| Start |
27308366:27308366(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.214C>A |
| AA Mutation |
p.Arg72Ser(p.R72S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000389032 |
| Start |
27322391:27322391(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1331A>C |
| AA Mutation |
p.Lys444Thr(p.K444T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |