Gene >> KRT19
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361566 |
| Start |
41527928:41527928(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.320A>G |
| AA Mutation |
p.Glu107Gly(p.E107G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361566 |
| Start |
41528240:41528240(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.8C>T |
| AA Mutation |
p.Ser3Phe(p.S3F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |