| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000498707 |
| Start |
64541191:64541191(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767643539
|
| CDS Mutation |
c.5425C>T |
| AA Mutation |
p.Arg1809Trp(p.R1809W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000498707 |
| Start |
64681332:64681332(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.548A>G |
| AA Mutation |
p.Tyr183Cys(p.Y183C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000498707 |
| Start |
64641867:64641867(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1837C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |