Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001347692 | SCV001541965 | uncertain significance | not provided | 2024-01-10 | criteria provided, single submitter | clinical testing | This variant, c.1705_1710del, results in the deletion of 2 amino acid(s) of the MKL1 protein (p.Ala569_Pro570del), but otherwise preserves the integrity of the reading frame. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with MKL1-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. |
Breakthrough Genomics, |
RCV001347692 | SCV005194475 | uncertain significance | not provided | criteria provided, single submitter | not provided | ||
Prevention |
RCV003928853 | SCV004742356 | benign | MRTFA-related disorder | 2020-01-10 | no assertion criteria provided | clinical testing | This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |