Gene >> APOA4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357780 |
| Start |
116822729:116822729(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.106A>G |
| AA Mutation |
p.Ser36Gly(p.S36G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000357780 |
| Start |
116821285:116821285(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.773C>G |
| AA Mutation |
p.Ala258Gly(p.A258G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |