Gene >> APOA4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357780 |
| Start |
116823146:116823146(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs180917395
|
| CDS Mutation |
c.46G>A |
| AA Mutation |
p.Ala16Thr(p.A16T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357780 |
| Start |
116821067:116821067(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.991C>T |
| AA Mutation |
p.Pro331Ser(p.P331S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |