| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000294517 |
| Start |
33084038:33084038(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148628180
|
| CDS Mutation |
c.190C>T |
| AA Mutation |
p.Arg64Trp(p.R64W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000294517 |
| Start |
33096805:33096805(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.852C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000294517 |
| Start |
33094674:33094674(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.714C>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |