Gene >> EDN2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000372587 |
| Start |
41484101:41484101(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.167A>G |
| AA Mutation |
p.Asp56Gly(p.D56G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000372587 |
| Start |
41479450:41479450(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764912588
|
| CDS Mutation |
c.496C>T |
| AA Mutation |
p.Arg166Trp(p.R166W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |