ClinVar Miner

List of variants reported as benign for ataxia-telangiectasia-like disorder 1

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 34
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HGVS dbSNP
NM_005590.4(MRE11):c.315-14_315-13dup rs35062043
NM_005591.3(MRE11):c.*1083T>C rs118070493
NM_005591.3(MRE11):c.*1766G>C rs13447752
NM_005591.3(MRE11):c.*183G>A rs13447745
NM_005591.3(MRE11):c.*2067A>G rs13447755
NM_005591.3(MRE11):c.*2501A>G rs2155209
NM_005591.3(MRE11):c.*2662A>G rs13447759
NM_005591.3(MRE11):c.*2699A>T rs13447760
NM_005591.3(MRE11):c.*442A>G rs1061956
NM_005591.3(MRE11):c.*511G>A rs13447749
NM_005591.3(MRE11):c.-106+5G>A rs1805363
NM_005591.3(MRE11):c.-178G>A rs1805360
NM_005591.3(MRE11):c.1002C>G (p.Ser334Arg) rs115244417
NM_005591.3(MRE11):c.1032T>G (p.Leu344=) rs11020793
NM_005591.3(MRE11):c.1098+17T>C rs1805365
NM_005591.3(MRE11):c.121G>A (p.Asp41Asn) rs116679717
NM_005591.3(MRE11):c.1225+19T>C rs641936
NM_005591.3(MRE11):c.1491C>T (p.Ile497=) rs199634245
NM_005591.3(MRE11):c.1780A>G (p.Arg594Gly) rs576878377
NM_005591.3(MRE11):c.1783+5G>C rs142082313
NM_005591.3(MRE11):c.1994+10G>A rs1805366
NM_005591.3(MRE11):c.2071-53G>T rs13447742
NM_005591.3(MRE11):c.2092A>G (p.Met698Val) rs1805362
NM_005591.3(MRE11):c.315-4del rs35062043
NM_005591.3(MRE11):c.426C>T (p.Asp142=) rs3218740
NM_005591.3(MRE11):c.771A>G (p.Glu257=) rs13447632
NM_005591.3(MRE11):c.81G>A (p.Glu27=) rs190031653
NM_005591.3(MRE11):c.822T>C (p.Leu274=) rs137868143
NM_005591.3(MRE11):c.969A>G (p.Pro323=) rs13447633
NM_005591.4(MRE11):c.*2053T>C
NM_005591.4(MRE11):c.*2466T>C
NM_005591.4(MRE11):c.1475C>A (p.Ala492Asp) rs61749249
NM_005591.4(MRE11):c.315-14dup rs35062043
NM_005591.4(MRE11):c.403-6G>A rs535801

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