Gene >> KRT17
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311208 |
| Start |
41620771:41620771(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374932182
|
| CDS Mutation |
c.1069C>T |
| AA Mutation |
p.Arg357Cys(p.R357C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311208 |
| Start |
41622423:41622423(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.604G>T |
| AA Mutation |
p.Ala202Ser(p.A202S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |