Gene >> PHEX
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379374 |
| Start |
22099099:22099099(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs768400503
|
| CDS Mutation |
c.1027G>A |
| AA Mutation |
p.Val343Ile(p.V343I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000379374 |
| Start |
22111529:22111529(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1142G>A |
| AA Mutation |
p.Arg381His(p.R381H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |