| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000374656 |
| Start |
33212374:33212374(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1196A>G |
| AA Mutation |
p.Tyr399Cys(p.Y399C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000374656 |
| Start |
33211838:33211838(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.955C>T |
| AA Mutation |
p.Pro319Ser(p.P319S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000374656 |
| Start |
33211515:33211515(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.813G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |