ClinVar Miner

List of variants in gene MRE11 reported as benign for not provided

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_005591.4(MRE11):c.153+144T>C rs608452 0.96955
NM_005591.4(MRE11):c.1327-273T>C rs496190 0.52594
NM_005591.4(MRE11):c.20+141G>A rs496797 0.51033
NM_005591.4(MRE11):c.-106+375T>C rs524350 0.51020
NM_005591.4(MRE11):c.-105-279C>T rs684507 0.49617
NM_005591.4(MRE11):c.1784-66A>G rs1014666 0.47713
NM_005591.4(MRE11):c.1868-273G>A rs500558 0.46121
NM_005591.4(MRE11):c.20+28G>A rs497763 0.42216
NM_005591.4(MRE11):c.1225+19T>C rs641936 0.36577
NM_005591.4(MRE11):c.1099-163G>A rs640627 0.31213
NM_005591.4(MRE11):c.403-112T>C rs680695 0.28999
NM_005591.4(MRE11):c.403-6G>A rs535801 0.28996
NM_005591.4(MRE11):c.*2501A>G rs2155209 0.27303
NM_005591.4(MRE11):c.659+107A>G rs13447623 0.18535
NM_005591.4(MRE11):c.1564-286A>C rs7947058 0.11661
NM_005591.4(MRE11):c.1783+270C>G rs12222920 0.11614
NM_005591.4(MRE11):c.-106+400G>C rs11825497 0.11435
NM_005591.4(MRE11):c.660-309A>G rs12273275 0.09580
NM_005591.4(MRE11):c.1017+284C>T rs3819119 0.07705
NM_005591.4(MRE11):c.1098+289G>C rs78716391 0.07444
NM_005591.4(MRE11):c.-106+5G>A rs1805363 0.06142
NM_005591.4(MRE11):c.1098+212T>C rs35931890 0.04843
NM_005591.4(MRE11):c.1098+204C>G rs35101429 0.04826
NM_005591.3(MRE11):c.-178G>A rs1805360 0.03996
NM_005591.4(MRE11):c.20+168dup rs13447586 0.03996
NM_005591.4(MRE11):c.1783+119A>C rs13447695 0.03651
NM_005591.4(MRE11):c.545-241T>C rs13447620 0.03390
NM_005591.4(MRE11):c.1868-133C>G rs13447713 0.03338
NM_005591.4(MRE11):c.21-143G>C rs1009455 0.03281
NM_005591.4(MRE11):c.-106+315G>T rs1009456 0.03266
NM_005591.4(MRE11):c.314+92A>G rs79462788 0.03262
NM_005591.4(MRE11):c.1099-217A>G rs104895017 0.01545
NM_005591.4(MRE11):c.1002C>G (p.Ser334Arg) rs115244417 0.01348
NM_005591.4(MRE11):c.1994+10G>A rs1805366 0.01130
NM_005591.4(MRE11):c.1326+99T>A rs13447660 0.01051
NM_005591.4(MRE11):c.1032T>G (p.Leu344=) rs11020793 0.00960
NM_005591.4(MRE11):c.1225+23G>T rs139950536 0.00631
NM_005591.4(MRE11):c.2092A>G (p.Met698Val) rs1805362 0.00548
NM_005591.4(MRE11):c.1225+39A>G rs13447650 0.00354
NM_005591.4(MRE11):c.771A>G (p.Glu257=) rs13447632 0.00301
NM_005591.4(MRE11):c.1783+5G>C rs142082313 0.00284
NM_005591.4(MRE11):c.969A>G (p.Pro323=) rs13447633 0.00258
NM_005591.4(MRE11):c.545-44C>T rs13447621 0.00165
NM_005591.4(MRE11):c.426C>T (p.Asp142=) rs3218740 0.00109
NM_005591.4(MRE11):c.120C>T (p.Leu40=) rs1805364 0.00066
NM_005591.4(MRE11):c.2052T>C (p.Val684=) rs367767415 0.00015
NM_005591.4(MRE11):c.81G>A (p.Glu27=) rs190031653 0.00006
NC_000011.10:g.94493932G>T rs12708334
NC_000011.10:g.94493959C>A rs11020802
NM_005591.4(MRE11):c.*660_*663dup
NM_005591.4(MRE11):c.1098+17T>C rs1805365
NM_005591.4(MRE11):c.1099-26G>C rs115448201
NM_005591.4(MRE11):c.1226-101C>A rs529126
NM_005591.4(MRE11):c.1226-255C>T rs7112263
NM_005591.4(MRE11):c.1326+235_1326+237del rs13447661
NM_005591.4(MRE11):c.1501-178del rs3832746
NM_005591.4(MRE11):c.1564-228del rs56850566
NM_005591.4(MRE11):c.1564-251_1564-250dup rs56850566
NM_005591.4(MRE11):c.1564-251dup rs56850566
NM_005591.4(MRE11):c.1868-85_1868-84del rs13447714
NM_005591.4(MRE11):c.1994+298G>C rs113009211
NM_005591.4(MRE11):c.314+300dup rs759826711
NM_005591.4(MRE11):c.315-14dup rs35062043
NM_005591.4(MRE11):c.315-4del rs35062043
NM_005591.4(MRE11):c.37T>A (p.Phe13Ile) rs149101834
NM_005591.4(MRE11):c.403-107G>A rs13447612
NM_005591.4(MRE11):c.846-60T>A rs610611

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