Gene >> AGO2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220592 |
| Start |
140585293:140585293(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201542441
|
| CDS Mutation |
c.41C>T |
| AA Mutation |
p.Pro14Leu(p.P14L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000220592 |
| Start |
140557220:140557220(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.895G>A |
| AA Mutation |
p.Glu299Lys(p.E299K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |