ClinVar Miner

Submissions for variant NM_001845.6(COL4A1):c.3497G>T (p.Gly1166Val) (rs1085307982)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000489567 SCV000577772 likely pathogenic not provided 2015-05-21 criteria provided, single submitter clinical testing The G1166V variant in the COL4A1 gene has not been published as a pathogenic variant, nor has it been reported as a benign polymorphism to our knowledge. The G1166V variant was not observed in approximately 6500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The G1166V variant is a conservative amino acid substitution, which is not likely to impact secondary protein structure as these residues share similar properties. This substitution occurs in the Triple-helical region at a position that is conserved across species. In silico analysis predicts this variant is probably damaging to the protein structure/function. The G1166V variant is a strong candidate for a disease-causing variant, however the possibility it may be a rare benign variant cannot be excluded.

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