ClinVar Miner

Submissions for variant NM_001845.6(COL4A1):c.2969G>T (p.Gly990Val) (rs1594550371)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000822448 SCV000963249 likely pathogenic not provided 2018-12-20 criteria provided, single submitter clinical testing This sequence change replaces glycine with valine at codon 990 of the COL4A1 protein (p.Gly990Val). The glycine residue is highly conserved and there is a moderate physicochemical difference between glycine and valine. This variant is not present in population databases (ExAC no frequency). This variant has been observed in an individual with clinical features of COL4A1-related disease (PMID: 26120313). Glycine residues within the Gly-Xaa-Yaa repeats of the triple helix domain are required for the structure and stability of fibrillar collagens (PMID: 7695699, 8218237, 19344236). In COL4A1, missense variants at these glycine residues are significantly enriched in individuals with disease (PMID: 10612821) compared to the general population (ExAC). In summary, this variant is a missense change affecting a residue that is known to be critical for normal protein structure, stability and function (PMID: 7695699, 8218237, 19344236). This type of missense change is also highly enriched in affected individuals and expected to be pathogenic (PMID: 10612821). However, without additional functional and/or genetic data, this variant has been classified as Likely Pathogenic.

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