ClinVar Miner

Submissions for variant NM_005732.4(RAD50):c.1353_1356del (p.Ser451fs)

dbSNP: rs1272811865
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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 RCV001011088 SCV001171369 pathogenic Hereditary cancer-predisposing syndrome 2022-08-19 criteria provided, single submitter clinical testing The c.1353_1356delTAAG pathogenic mutation, located in coding exon 9 of the RAD50 gene, results from a deletion of 4 nucleotides at nucleotide positions 1353 to 1356, causing a translational frameshift with a predicted alternate stop codon. 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.
Invitae RCV001011088 SCV001580289 pathogenic Hereditary cancer-predisposing syndrome 2023-03-15 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 818961). This variant has not been reported in the literature in individuals affected with RAD50-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.01%). This sequence change creates a premature translational stop signal (p.Ser451Argfs*6) in the RAD50 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in RAD50 are known to be pathogenic (PMID: 19409520).

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