| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380191 |
| Start |
5768347:5768347(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.857A>G |
| AA Mutation |
p.Tyr286Cys(p.Y286C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380191 |
| Start |
5768267:5768267(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.937G>A |
| AA Mutation |
p.Asp313Asn(p.D313N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000380191 |
| Start |
5766039:5766039(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1305G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |