ClinVar Miner

List of variants in gene combination ATM, C11orf65 reported as likely benign by Counsyl

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Gene type:
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Total variants: 15
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HGVS dbSNP
NM_000051.3(ATM):c.5918+16A>G rs3092911
NM_000051.3(ATM):c.6007-10A>G rs373395916
NM_000051.3(ATM):c.6088A>G (p.Ile2030Val) rs145847315
NM_000051.3(ATM):c.6396A>G (p.Leu2132=) rs370537345
NM_000051.3(ATM):c.6888A>T (p.Ala2296=) rs200735689
NM_000051.3(ATM):c.7131T>C (p.Asp2377=) rs373309822
NM_000051.3(ATM):c.7494T>C (p.Ser2498=) rs34393781
NM_000051.3(ATM):c.7515+20A>G rs80124497
NM_000051.3(ATM):c.7785T>C (p.Asp2595=) rs34838175
NM_000051.3(ATM):c.7788+8G>T rs112775908
NM_000051.3(ATM):c.8010+185_8010+186delCC rs984385407
NM_000051.3(ATM):c.8100A>G (p.Lys2700=) rs778601472
NM_000051.3(ATM):c.8584+10T>C rs373321041
NM_000051.3(ATM):c.8629T>C (p.Leu2877=) rs730881279
NM_000051.3(ATM):c.8987+10A>G rs1060504308

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