| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000359156 |
| Start |
7482694:7482694(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3196G>T |
| AA Mutation |
p.Val1066Phe(p.V1066F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000359156 |
| Start |
7486668:7486668(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2289A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000359156 |
| Start |
7487657:7487657(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1752C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |