Gene STRC 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: STRC
Disorder: Deafness, non-syndromic
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 STRC gene based on the Emirati cohort dataset.
| id |
Chromosome Position |
Gene Name |
HGVS c. (Clinically Relevant) |
HGVS p. (Clinically Relevant) |
Allele Count |
Allele Frequency |
| 463 |
43891923 |
STRC |
NM_153700.2:c.5275C>T |
NP_714544.1:p.Arg1759Ter |
1 |
0.000419% |
| 464 |
43897503 |
STRC |
NM_153700.2:c.3889dupC |
NP_714544.1:p.Leu1297Profs*89 |
1 |
0.000419% |
| 465 |
43903435 |
STRC |
NM_153700.2:c.3217C>T |
NP_714544.1:p.Arg1073Ter |
1 |
0.000419% |
