ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.632dup (p.Gly212fs)

dbSNP: rs1060501779
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000657344 SCV000779076 pathogenic not provided 2017-06-22 criteria provided, single submitter clinical testing This duplication of one nucleotide in BRIP1 is denoted c.632dupC at the cDNA level and p.Gly212TrpfsX5 (G212WfsX5) at the protein level. The normal sequence, with the base that is duplicated in brackets, is GCCCC[dupC]TGGC. The duplication causes a frameshift which changes a Glycine to a Tryptophan at codon 212, and creates a premature stop codon at position 5 of the new reading frame. Although this variant has not, to our knowledge, been reported in the literature, it is predicted to cause loss of normal protein function through either protein truncation or nonsense-mediated mRNA decay. We consider this variant to be pathogenic.

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