ClinVar Miner

List of variants in gene combination ATM, C11orf65 reported as benign for Hereditary cancer-predisposing syndrome

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Total variants: 24
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HGVS dbSNP
NM_000051.3(ATM):c.5793T>C (p.Ala1931=) rs3092910
NM_000051.3(ATM):c.5948G>A (p.Ser1983Asn) rs659243
NM_000051.3(ATM):c.6088A>G (p.Ile2030Val) rs145847315
NM_000051.3(ATM):c.6095+15T>C rs3212321
NM_000051.3(ATM):c.6235G>A (p.Val2079Ile) rs1800060
NM_000051.3(ATM):c.6347+31del rs58978479
NM_000051.3(ATM):c.6348-8T>C rs730881292
NM_000051.3(ATM):c.6437G>C (p.Ser2146Thr) rs56815840
NM_000051.3(ATM):c.6572+12G>T rs3218677
NM_000051.3(ATM):c.6919C>T (p.Leu2307Phe) rs56009889
NM_000051.3(ATM):c.6995T>C (p.Leu2332Pro) rs4988111
NM_000051.3(ATM):c.7313C>T (p.Thr2438Ile) rs147604227
NM_000051.3(ATM):c.7390T>C (p.Cys2464Arg) rs55801750
NM_000051.3(ATM):c.7629+13G>A rs563651647
NM_000051.3(ATM):c.7630-17T>C rs116047570
NM_000051.3(ATM):c.7927+13dup rs587781324
NM_000051.3(ATM):c.8010+186C>T rs227060
NM_000051.3(ATM):c.8269-14A>T rs114320959
NM_000051.3(ATM):c.8419-19A>G rs12279930
NM_000051.3(ATM):c.8786+8A>C rs4986839
NM_000051.3(ATM):c.8851-973A>C rs170548
NM_000051.3(ATM):c.8921C>T (p.Pro2974Leu) rs139379666
NM_000051.3(ATM):c.9006C>T (p.Phe3002=) rs540172506
NM_000051.3(ATM):c.9086G>A (p.Gly3029Asp) rs201199629

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