ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.4343G>A (p.Ser1448Asn) (rs80357354)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000215083 SCV000277368 likely benign Hereditary cancer-predisposing syndrome 2015-07-16 criteria provided, single submitter clinical testing
GeneDx RCV000483990 SCV000571680 uncertain significance not provided 2016-09-14 criteria provided, single submitter clinical testing This variant is denoted BRCA1 c.4343G>A at the cDNA level, p.Ser1448Asn (S1448N) at the protein level, and results in the change of a Serine to an Asparagine (AGC>AAC). Using alternate nomenclature, this variant would be defined as BRCA1 4462G>A. This variant has not, to our knowledge, been published in the literature as pathogenic or benign. BRCA1 Ser1448Asn was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, suggesting it is not a common benign variant in these populations. Since Serine and Asparagine share similar properties, this is considered a conservative amino acid substitution. BRCA1 Ser1448Asn occurs at a position that is not conserved and is located in the SCD domain and the regions of interaction with ATM, CHEK2, CDK2 and BRCA2 (Chen 1998, Narod 2004, Clark 2012). In silico analyses predict that this variant is unlikely to alter protein structure or function. Based on currently available evidence, it is unclear whether BRCA1 Ser1448Asn is a pathogenic or benign variant. We consider it to be a variant of uncertain significance.
Breast Cancer Information Core (BIC) (BRCA1) RCV000112320 SCV000145063 uncertain significance Breast-ovarian cancer, familial 1 2002-05-29 no assertion criteria provided clinical testing

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