| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000319715 |
| Start |
24570365:24570365(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767099633
|
| CDS Mutation |
c.3675A>G |
| AA Mutation |
p.Ile1225Met(p.I1225M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000319715 |
| Start |
24567390:24567390(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1837A>G |
| AA Mutation |
p.Thr613Ala(p.T613A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000319715 |
| Start |
24569885:24569885(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3195G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |