| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000360428 |
| Start |
31025864:31025864(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs137869359
|
| CDS Mutation |
c.526C>T |
| AA Mutation |
p.Arg176Cys(p.R176C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360428 |
| Start |
31030993:31030993(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.334C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000360428 |
| Start |
31022489:31022489(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs573762324
|
| CDS Mutation |
c.789G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |