| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000618562 |
| Start |
176687490:176687490(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.842G>A |
| AA Mutation |
p.Gly281Glu(p.G281E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000618562 |
| Start |
176729553:176729553(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.341A>T |
| AA Mutation |
p.Tyr114Phe(p.Y114F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000618562 |
| Start |
176711534:176711534(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.669C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |