Gene >> KRT19
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361566 |
| Start |
41527965:41527965(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.283C>A |
| AA Mutation |
p.Leu95Met(p.L95M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361566 |
| Start |
41523879:41523879(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1067G>A |
| AA Mutation |
p.Ser356Asn(p.S356N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |