ClinVar Miner

Submissions for variant NM_005732.4(RAD50):c.136A>G (p.Ile46Val)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003239298 SCV003936816 uncertain significance Familial cancer of breast 2023-07-05 criteria provided, single submitter clinical testing This sequence change replaces leucine with valine at codon 46 of the RAD50 protein (p.Ile46Val). This variant is not present in population databases (gnomAD). This variant has not been reported in the literature in individuals with p.RAD50-related conditions. In-silico predictions show conflicting computational verdict based on 6 benign predictions from PROVEAN , MVP , M-CAP , FATHMM , DEOGEN2 and BLOSUM vs 6 pathogenic prediction from FATHMM-MKL , LRT, Mutation assessor , SIFT and PolyPhen the position is not strongly conserved (PhyloP=6.58) . This variant not reported in ClinVar , same amino acid reported as (p.Ile46Thr) and (p.Ile46Asn) of which both reported as variant of uncertain significance .

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