Gene >> PLXNA4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000321063 |
| Start |
132168551:132168551(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs369917118
|
| CDS Mutation |
c.4039C>T |
| AA Mutation |
p.Arg1347Cys(p.R1347C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000321063 |
| Start |
132174876:132174876(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3919C>A |
| AA Mutation |
p.Leu1307Met(p.L1307M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |