Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Clinical Genomics Laboratory, |
RCV003457221 | SCV004177113 | uncertain significance | Cardiofaciocutaneous syndrome 3 | 2023-10-26 | criteria provided, single submitter | clinical testing | A MAP2K1 c.1023-4T>A variant was identified at a near heterozygous allelic fraction of 49%, which may be consistent with germline origin. To our knowledge, this variant has not been reported in the medical literature in relation to MAP2K1-related disease. This variant is only observed on 2/152,174 alleles in the general population (gnomAD v.3.1.2), indicating it is not a common variant. Computational predictors indicate that the variant has no impact on splicing, evidence that this variant may not have a damaging effect on MAP2K1 function. Due to limited information, and based on ACMG/AMP guidelines for variant interpretation (Richards S et al., PMID: 25741868) and based on ClinGen's RASopathy expert panel (Gelb BD et al. PMID: 29493581), the clinical significance of this variant is uncertain at this time. |
Labcorp Genetics |
RCV003655429 | SCV004508825 | likely benign | RASopathy | 2022-12-16 | criteria provided, single submitter | clinical testing |