| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000377346 |
| Start |
9720854:9720854(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1634C>T |
| AA Mutation |
p.Ala545Val(p.A545V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000377346 |
| Start |
9716493:9716493(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.654C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000377346 |
| Start |
9719989:9719989(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1311C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |