Gene >> KRT31
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251645 |
| Start |
41395065:41395065(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.880G>A |
| AA Mutation |
p.Asp294Asn(p.D294N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000251645 |
| Start |
41395530:41395530(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.682A>G |
| AA Mutation |
p.Thr228Ala(p.T228A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |