Gene >> NME1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000393196 |
| Start |
51155755:51155755(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765050521
|
| CDS Mutation |
c.101G>A |
| AA Mutation |
p.Arg34His(p.R34H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000393196 |
| Start |
51161772:51161772(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.386A>T |
| AA Mutation |
p.Glu129Val(p.E129V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |