Gene >> PLXNC1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000258526 |
| Start |
94247922:94247922(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749923591
|
| CDS Mutation |
c.2408C>T |
| AA Mutation |
p.Ala803Val(p.A803V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000258526 |
| Start |
94279545:94279545(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3671T>C |
| AA Mutation |
p.Val1224Ala(p.V1224A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |