ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.304C>T (p.Gln102Ter)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV002444091 SCV002752910 pathogenic Hereditary cancer-predisposing syndrome 2022-06-15 criteria provided, single submitter clinical testing The p.Q102* pathogenic mutation (also known as c.304C>T), located in coding exon 3 of the BRIP1 gene, results from a C to T substitution at nucleotide position 304. This changes the amino acid from a glutamine to a stop codon within coding exon 3. This variant is considered to be rare based on population cohorts in the Genome Aggregation Database (gnomAD). This alteration is expected to result in loss of function by premature protein truncation or nonsense-mediated mRNA decay. As such, this alteration is interpreted as a disease-causing mutation.
Myriad Genetics, Inc. RCV003336755 SCV004045100 pathogenic Familial cancer of breast 2023-05-30 criteria provided, single submitter clinical testing This variant is considered pathogenic. This variant creates a termination codon and is predicted to result in premature protein truncation.

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