Gene >> AOC2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253799 |
| Start |
42844996:42844996(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs775599309
|
| CDS Mutation |
c.370G>A |
| AA Mutation |
p.Val124Ile(p.V124I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253799 |
| Start |
42845968:42845968(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1342G>A |
| AA Mutation |
p.Gly448Ser(p.G448S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |