| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000500728 |
| Start |
3518100:3518100(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs777028219
|
| CDS Mutation |
c.685C>T |
| AA Mutation |
p.Arg229Cys(p.R229C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000500728 |
| Start |
3524950:3524950(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770350585
|
| CDS Mutation |
c.306C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000500728 |
| Start |
3514911:3514911(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776519916
|
| CDS Mutation |
c.852C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |