Gene >> MX2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330714 |
| Start |
41398919:41398919(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1172G>T |
| AA Mutation |
p.Gly391Val(p.G391V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000330714 |
| Start |
41398961:41398961(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368866145
|
| CDS Mutation |
c.1214G>A |
| AA Mutation |
p.Arg405Gln(p.R405Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |