Gene >> KRT16
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000301653 |
| Start |
41611200:41611200(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.802G>A |
| AA Mutation |
p.Gly268Arg(p.G268R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000301653 |
| Start |
41612503:41612503(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200450332
|
| CDS Mutation |
c.186C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |