ClinVar Miner

Submissions for variant NM_000038.6(APC):c.6232C>G (p.Leu2078Val)

dbSNP: rs786203610
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000166999 SCV000217821 uncertain significance Hereditary cancer-predisposing syndrome 2014-12-02 criteria provided, single submitter clinical testing The p.L2078V variant (also known as c.6232C>G), located in coding exon 15 of the APC gene, results from a C to G substitution at nucleotide position 6232. The leucine at codon 2078 is replaced by valine, an amino acid with highly similar properties. This variant was not reported in population based cohorts in the following databases: Database of Single Nucleotide Polymorphisms (dbSNP), NHLBI Exome Sequencing Project (ESP), and 1000 Genomes Project. In the ESP, this variant was not observed in 6502 samples (13004 alleles) with coverage at this position. To date, this alteration has been detected with an allele frequency of approximately 0.01% (greater than 13000 alleles tested) in our clinical cohort. This amino acid position is highly conserved in available vertebrate species. In addition, this alteration is predicted to be tolerated by in silico analysis. Since supporting evidence is limited at this time, the clinical significance of p.L2078V remains unclear.

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