| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262483 |
| Start |
6478650:6478650(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.674C>G |
| AA Mutation |
p.Ser225Cys(p.S225C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262483 |
| Start |
6483597:6483597(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs367702668
|
| CDS Mutation |
c.507C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262483 |
| Start |
6470287:6470287(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1746A>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |