Gene MYO15A 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: MYO15A
Disorder: Deafness, non-syndromic, autosomal recessive
Allele Frequency: 0.000837521
Carrier Rate: 0.00167364
Max At-Risk Couples rate: 0.0000028
The table below lists all clinically relevant variants identified in the MYO15A gene based on the Emirati cohort dataset.
| id |
Chromosome Position |
Gene Name |
HGVS c. (Clinically Relevant) |
HGVS p. (Clinically Relevant) |
Allele Count |
Allele Frequency |
| 513 |
18022312 |
MYO15A |
NM_016239.4:c.202delC |
NP_057323.3:p.Gln68Argfs*20 |
1 |
0.000419% |
| 514 |
18039061 |
MYO15A |
NM_016239.4:c.4519C>T |
NP_057323.3:p.Arg1507Ter |
1 |
0.000419% |
