| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262626 |
| Start |
35060373:35060373(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.481G>T |
| AA Mutation |
p.Asp161Tyr(p.D161Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262626 |
| Start |
35049489:35049489(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.133A>T |
| AA Mutation |
p.Arg45Trp(p.R45W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262626 |
| Start |
35065876:35065876(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1059C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |