| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000250378 |
| Start |
24507468:24507468(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs138432864
|
| CDS Mutation |
c.97C>T |
| AA Mutation |
p.Arg33Cys(p.R33C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000250378 |
| Start |
24506124:24506124(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.504A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000250378 |
| Start |
24507430:24507430(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.135C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |