ClinVar Miner

Submissions for variant NM_003072.5(SMARCA4):c.3556G>A (p.Ala1186Thr)

dbSNP: rs1085307556
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000490168 SCV000576717 pathogenic not provided 2017-04-20 criteria provided, single submitter clinical testing The A1186T variant in the SMARCA4 gene has not been reported previously as a germline pathogenic variant, nor as a benign variant, to our knowledge. The A1186T variant is not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The A1186T variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs within the HELICc domain at a position that is conserved across species (Witkowski et al., 2014). In silico analysis predicts this variant is probably damaging to the protein structure/function. We interpret A1186T as a pathogenic variant

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