| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000282928 |
| Start |
147410940:147410940(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.828T>G |
| AA Mutation |
p.Cys276Trp(p.C276W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000282928 |
| Start |
147410577:147410577(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.465G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000282928 |
| Start |
147411006:147411006(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.894C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |