Gene >> SNCG
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000372017 |
| Start |
86960124:86960124(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs371074090
|
| CDS Mutation |
c.287G>A |
| AA Mutation |
p.Arg96His(p.R96H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000372017 |
| Start |
86960124:86960124(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs371074090
|
| CDS Mutation |
c.287G>T |
| AA Mutation |
p.Arg96Leu(p.R96L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |