ClinVar Miner

Submissions for variant NM_001291303.3(FAT4):c.14120C>A (p.Pro4707His)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genomics Laboratory, Washington University in St. Louis RCV004560386 SCV005047083 uncertain significance Hennekam lymphangiectasia-lymphedema syndrome 2 2024-05-08 criteria provided, single submitter clinical testing A FAT4 c.14120C>A (p.Pro4707His) variant was identified at an allelic fraction of 50.1%, which may be consistent with it being of germline origin. This variant, to our knowledge, has not been reported in the medical literature. It is only observed on 2/152,216 alleles in the general population (gnomAD v.4.1.0), indicating that it is not a common variant. Computational predictors are uncertain as to the impact of this variant on FAT4 function. Due to limited information, and based on ACMG/AMP guidelines for variant interpretation (Richards S et al., PMID: 25741868), the clinical significance of this variant is uncertain at this time.

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