Gene >> GRAP2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344138 |
| Start |
39970912:39970912(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774420692
|
| CDS Mutation |
c.821G>A |
| AA Mutation |
p.Arg274Gln(p.R274Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000344138 |
| Start |
39947138:39947138(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.32C>A |
| AA Mutation |
p.Ala11Asp(p.A11D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |