ClinVar Miner

Submissions for variant NM_133433.4(NIPBL):c.1273C>G (p.Gln425Glu) (rs1554015229)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000497520 SCV000589420 uncertain significance not provided 2018-09-06 criteria provided, single submitter clinical testing The Q425E variant in the NIPBL gene has not been published as a pathogenic variant, nor has it been reported as a benign polymorphism to our knowledge. The Q425E 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 variant in these populations. The Q425E variant is a semi-conservative amino acid substitution, which occurs in the Gln-rich Compositional bias region at a position that is conserved through mammals. In silico analysis predicts this variant likely does not alter the protein structure/function. We interpret Q425E as a variant of unknown significance.

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