ClinVar Miner

Submissions for variant NM_000088.4(COL1A1):c.3379G>C (p.Gly1127Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001285199 SCV001471597 likely pathogenic none provided 2019-08-02 criteria provided, single submitter clinical testing The COL1A1 c.3379G>C; p.Gly1127Arg variant, to our knowledge, is not reported in the medical literature or gene specific databases. This variant is also absent from general population databases (Exome Variant Server, Genome Aggregation Database), indicating it is not a common polymorphism. The glycine at codon 1127 is highly conserved, and computational analyses (SIFT, PolyPhen-2) predict that this variant is deleterious. Additionally, another variant at this codon (c.3380G>A; p.Gly1127Asp) has been reported as a de novo variant in at least one individual with a type I collagenopathy and is considered pathogenic (Lee 2017). This codon is located in a triple helix repeat domain, and glycine substitutions are the most frequent pathogenic alterations in this region (Ben Amor 2011). Based on available information, the p.Gly1127Arg variant is considered to be likely pathogenic. References: Ben Amor I et al. Genotype-phenotype correlations in autosomal dominant osteogenesis imperfecta. J Osteoporos. 2011; 2011:540178. Lee JS et al. Severe hypotonia and postnatal growth impairment in a girl with a missense mutation in COL1A1: Implication of expanded phenotypic spectrum of type I collagenopathy. Brain Dev. 2017 Oct;39(9):799-803.

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