Gene >> KRT4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000551956 |
| Start |
52813863:52813863(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.196G>A |
| AA Mutation |
p.Ala66Thr(p.A66T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000551956 |
| Start |
52808333:52808333(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1086C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |