Gene PLEKHG5 Details
It offers a comprehensive overview of all clinically relevant variants linked to a specified gene. It provides detailed metrics for each variant, including chromosomal position, HGVS c. and p. notation, allele frequencies, carrier rates, and estimated metrics for at-risk couples. By combining gene-level statistics with specific variant-level data, this page enables an in-depth analysis of how particular genes contribute to disease, thus supporting both clinical interpretation and research efforts.
Gene: PLEKHG5
Disorder: Myopathy
Allele Frequency: 0.00125628
Carrier Rate: 0.00250941
Max At-Risk Couples rate: 0.0000063
The table below lists all clinically relevant variants identified in the PLEKHG5 gene based on the Emirati cohort dataset.
| id |
Chromosome Position |
Gene Name |
HGVS c. (Clinically Relevant) |
HGVS p. (Clinically Relevant) |
Allele Count |
Allele Frequency |
| 161 |
6529188 |
PLEKHG5 |
NM_020631.6:c.2163_2164insAA |
NP_065682.2:p.Glu722Lysfs*44 |
2 |
0.000838% |
| 346 |
6529238 |
PLEKHG5 |
NM_020631.6:c.2113delG |
NP_065682.2:p.Glu705Lysfs*60 |
1 |
0.000419% |
