Gene >> PKN1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000242783 |
| Start |
14470201:14470201(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2332A>G |
| AA Mutation |
p.Thr778Ala(p.T778A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000242783 |
| Start |
14467776:14467776(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1867C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |