ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.3797G>T (p.Ser1266Ile) (rs80357160)

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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 RCV000130110 SCV000184940 uncertain significance Hereditary cancer-predisposing syndrome 2013-12-24 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence
GeneDx RCV000236943 SCV000293882 uncertain significance not provided 2016-01-28 criteria provided, single submitter clinical testing This variant is denoted BRCA1 c.3797G>T at the cDNA level, p.Ser1266Ile (S1266I) at the protein level, and results in the change of a Serine to an Isoleucine (AGC>ATC). Using alternate nomenclature, this variant would be defined as BRCA1 3916G>T. This variant has not, to our knowledge, been published in the literature as pathogenic or benign. BRCA1 Ser1266Ile 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 Isoleucine differ in polarity, charge, size or other properties, this is considered a non-conservative amino acid substitution. BRCA1 Ser1266Ile occurs at a position that is not conserved and is not located in a known functional domain (UniProt, Paul 2014). In silico analyses are inconsistent regarding the effect this variant may have on protein structure and function. Based on currently available evidence, it is unclear whether BRCA1 Ser1266Ile is pathogenic or benign. We consider it to be a variant of uncertain significance.

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