ClinVar Miner

Submissions for variant NM_005334.3(HCFC1):c.2029-7_2029-6insTAA

dbSNP: rs1383257179
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000519421 SCV000619130 uncertain significance not provided 2019-01-18 criteria provided, single submitter clinical testing The c.2029-7_2029-6insAAT variant in the HCFC1 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. This variant results in the insertion of three nucleotides and is predicted to slightly damage the natural splice acceptor site of intron 11, which may cause abnormal gene splicing. The c.2029-7_2029-6insAAT variant is not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). We interpret c.2029-7_2029-6insAAT as a variant of uncertain significance.

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