ClinVar Miner

List of variants in gene MRE11 reported as uncertain significance for Ataxia-telangiectasia-like disorder 1

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Total variants: 161
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HGVS dbSNP
NC_000011.9:g.(?_94153285)_(94170407_?)del
NM_005591.3(MRE11):c.*1083T>C rs118070493
NM_005591.3(MRE11):c.*1086A>G rs886048752
NM_005591.3(MRE11):c.*1304A>T rs562083257
NM_005591.3(MRE11):c.*1366G>A rs146641719
NM_005591.3(MRE11):c.*1554C>G rs886048751
NM_005591.3(MRE11):c.*1661A>C rs539061083
NM_005591.3(MRE11):c.*1776C>T rs104895005
NM_005591.3(MRE11):c.*189G>A rs151287483
NM_005591.3(MRE11):c.*1933G>T rs104895004
NM_005591.3(MRE11):c.*2067A>G rs13447755
NM_005591.3(MRE11):c.*2106T>C rs886048750
NM_005591.3(MRE11):c.*2178A>C rs886048749
NM_005591.3(MRE11):c.*2258G>C rs886048748
NM_005591.3(MRE11):c.*2296A>G rs886048747
NM_005591.3(MRE11):c.*2320T>C rs886048746
NM_005591.3(MRE11):c.*2444A>G rs369336016
NM_005591.3(MRE11):c.*2452C>T rs574670712
NM_005591.3(MRE11):c.*2662A>G rs13447759
NM_005591.3(MRE11):c.*2703A>G rs766297244
NM_005591.3(MRE11):c.*313G>A rs886048758
NM_005591.3(MRE11):c.*447T>G rs886048757
NM_005591.3(MRE11):c.*628G>A rs142407545
NM_005591.3(MRE11):c.*650_*659dupTCTCTCTCTC rs201800515
NM_005591.3(MRE11):c.*654_*659dupTCTCTC rs201800515
NM_005591.3(MRE11):c.*656_*659dupTCTC rs201800515
NM_005591.3(MRE11):c.*658_*659delTC rs201800515
NM_005591.3(MRE11):c.*658_*659dupTC rs201800515
NM_005591.3(MRE11):c.*659_*660insTCTCTCTCCC rs373002609
NM_005591.3(MRE11):c.*659_*660insTCTCTCTCTCTCCC rs373002609
NM_005591.3(MRE11):c.*659_*660insTCTCTCTCTCTCTCCC rs373002609
NM_005591.3(MRE11):c.*660C>T rs591959
NM_005591.3(MRE11):c.*669C>G rs886048755
NM_005591.3(MRE11):c.*671C>T rs538218500
NM_005591.3(MRE11):c.*741A>G rs886048754
NM_005591.3(MRE11):c.*848A>G rs13447750
NM_005591.3(MRE11):c.*910dupT rs886048753
NM_005591.3(MRE11):c.*997A>G rs149208652
NM_005591.3(MRE11):c.-106+8C>T rs886048761
NM_005591.3(MRE11):c.1036A>G (p.Asn346Asp)
NM_005591.3(MRE11):c.1045C>T (p.Arg349Trp) rs570102851
NM_005591.3(MRE11):c.1046G>A (p.Arg349Gln) rs864622683
NM_005591.3(MRE11):c.1051C>T (p.Arg351Cys) rs757492041
NM_005591.3(MRE11):c.106A>G (p.Thr36Ala) rs774330292
NM_005591.3(MRE11):c.1073C>A (p.Pro358Gln) rs1430351329
NM_005591.3(MRE11):c.1090C>A (p.Arg364=) rs371077728
NM_005591.3(MRE11):c.1091G>T (p.Arg364Leu) rs140528613
NM_005591.3(MRE11):c.1097G>A (p.Arg366Gln) rs773968042
NM_005591.3(MRE11):c.1106A>G (p.Tyr369Cys) rs746283923
NM_005591.3(MRE11):c.1138C>T (p.Arg380Cys) rs766182900
NM_005591.3(MRE11):c.1145G>C (p.Ser382Thr) rs745769023
NM_005591.3(MRE11):c.1163G>A (p.Arg388Gln) rs587780134
NM_005591.3(MRE11):c.1187T>C (p.Ile396Thr) rs1555010863
NM_005591.3(MRE11):c.1190A>C (p.His397Pro) rs372657126
NM_005591.3(MRE11):c.1195T>A (p.Phe399Ile) rs904951211
NM_005591.3(MRE11):c.121G>A (p.Asp41Asn) rs116679717
NM_005591.3(MRE11):c.1225+10T>G rs863224734
NM_005591.3(MRE11):c.1238A>G (p.Asn413Ser) rs587782457
NM_005591.3(MRE11):c.123_125del (p.Asp41del) rs1555018284
NM_005591.3(MRE11):c.1261C>T (p.Pro421Ser) rs1398359004
NM_005591.3(MRE11):c.1268A>C (p.Glu423Ala) rs1565221498
NM_005591.3(MRE11):c.1280T>C (p.Leu427Ser) rs786203449
NM_005591.3(MRE11):c.1281A>T (p.Leu427Phe) rs1555009888
NM_005591.3(MRE11):c.1318G>T (p.Ala440Ser) rs773469981
NM_005591.3(MRE11):c.1327-9A>T rs766573839
NM_005591.3(MRE11):c.1334A>G (p.Gln445Arg) rs371730091
NM_005591.3(MRE11):c.1369G>A (p.Ala457Thr) rs1555009409
NM_005591.3(MRE11):c.1404T>C (p.Asp468=) rs368144567
NM_005591.3(MRE11):c.140C>T (p.Ala47Val) rs730880378
NM_005591.3(MRE11):c.1420G>A (p.Val474Met) rs778781414
NM_005591.3(MRE11):c.1448G>A (p.Arg483Gln) rs587781378
NM_005591.3(MRE11):c.1462C>G (p.Arg488Gly) rs375261439
NM_005591.3(MRE11):c.1463G>A (p.Arg488His) rs145377856
NM_005591.3(MRE11):c.1478T>G (p.Leu493Arg) rs786203158
NM_005591.3(MRE11):c.1480G>A (p.Glu494Lys) rs104895016
NM_005591.3(MRE11):c.1499A>T (p.Glu500Val) rs786203159
NM_005591.3(MRE11):c.1501-8T>G rs753131403
NM_005591.3(MRE11):c.1504C>T (p.Arg502Cys) rs186333183
NM_005591.3(MRE11):c.1545A>G (p.Glu515=) rs886048759
NM_005591.3(MRE11):c.1551T>G (p.Asp517Glu) rs1555008221
NM_005591.3(MRE11):c.1555G>T (p.Val519Phe) rs778116138
NM_005591.3(MRE11):c.1559G>A (p.Arg520His) rs753148077
NM_005591.3(MRE11):c.1563G>A (p.Glu521=) rs779250359
NM_005591.3(MRE11):c.1571C>G (p.Thr524Ser) rs876659237
NM_005591.3(MRE11):c.1574G>A (p.Arg525Lys) rs773275841
NM_005591.3(MRE11):c.1667A>G (p.Asn556Ser) rs144896235
NM_005591.3(MRE11):c.16G>C (p.Ala6Pro) rs1060501784
NM_005591.3(MRE11):c.1715G>A (p.Arg572Gln) rs200085146
NM_005591.3(MRE11):c.1718G>A (p.Gly573Glu) rs587781461
NM_005591.3(MRE11):c.1724G>A (p.Gly575Asp) rs376555330
NM_005591.3(MRE11):c.1724G>T (p.Gly575Val) rs376555330
NM_005591.3(MRE11):c.1727G>A (p.Arg576Gln) rs139461096
NM_005591.3(MRE11):c.1732G>T (p.Gly578Cys) rs547793891
NM_005591.3(MRE11):c.1736G>A (p.Gly579Glu) rs757916109
NM_005591.3(MRE11):c.1753G>A (p.Ala585Thr) rs754790440
NM_005591.3(MRE11):c.1758G>A (p.Ser586=) rs766372720
NM_005591.3(MRE11):c.1762G>A (p.Gly588Arg) rs1555005282
NM_005591.3(MRE11):c.1783+7A>G rs774520952
NM_005591.3(MRE11):c.1783+8C>G rs372784831
NM_005591.3(MRE11):c.1801A>C (p.Thr601Pro) rs1565211523
NM_005591.3(MRE11):c.1810C>T (p.Arg604Cys) rs750926542
NM_005591.3(MRE11):c.1811G>A (p.Arg604His) rs148637964
NM_005591.3(MRE11):c.1852A>G (p.Met618Val) rs375630981
NM_005591.3(MRE11):c.1853T>G (p.Met618Arg) rs748933763
NM_005591.3(MRE11):c.1858A>G (p.Ile620Val) rs144070976
NM_005591.3(MRE11):c.1868-4C>A rs768257868
NM_005591.3(MRE11):c.1875A>C (p.Lys625Asn) rs907660509
NM_005591.3(MRE11):c.1892C>G (p.Pro631Arg) rs1555002427
NM_005591.3(MRE11):c.18A>T (p.Ala6=) rs758314845
NM_005591.3(MRE11):c.2023A>T (p.Met675Leu) rs756418071
NM_005591.3(MRE11):c.202T>C (p.Ser68Pro) rs1555017253
NM_005591.3(MRE11):c.2033G>A (p.Ser678Asn) rs781684108
NM_005591.3(MRE11):c.2042C>T (p.Ser681Leu) rs587782166
NM_005591.3(MRE11):c.2071_2073GAT[6] (p.Asp695dup) rs779409748
NM_005591.3(MRE11):c.2096A>G (p.Asn699Ser) rs876660153
NM_005591.3(MRE11):c.2099C>G (p.Thr700Ser) rs374685908
NM_005591.3(MRE11):c.21-6_26delATATAGTGATGA rs587780138
NM_005591.3(MRE11):c.231G>T (p.Glu77Asp)
NM_005591.3(MRE11):c.239G>T (p.Arg80Ile) rs587782472
NM_005591.3(MRE11):c.274G>A (p.Glu92Lys) rs587780139
NM_005591.3(MRE11):c.302T>A (p.Phe101Tyr) rs1555017179
NM_005591.3(MRE11):c.314+6T>C rs864622413
NM_005591.3(MRE11):c.32A>G (p.Asn11Ser) rs1555018337
NM_005591.3(MRE11):c.331T>G (p.Tyr111Asp) rs1555015455
NM_005591.3(MRE11):c.337G>A (p.Asp113Asn) rs876659042
NM_005591.3(MRE11):c.33C>A (p.Asn11Lys) rs746088302
NM_005591.3(MRE11):c.358A>G (p.Ile120Val) rs372131911
NM_005591.3(MRE11):c.365T>G (p.Val122Gly) rs1565234530
NM_005591.3(MRE11):c.37T>C (p.Phe13Leu) rs149101834
NM_005591.3(MRE11):c.391G>T (p.Asp131Tyr) rs368403414
NM_005591.3(MRE11):c.426C>T (p.Asp142=) rs3218740
NM_005591.3(MRE11):c.44T>C (p.Ile15Thr)
NM_005591.3(MRE11):c.454C>T (p.His152Tyr) rs876659023
NM_005591.3(MRE11):c.463C>T (p.Arg155Cys) rs587782512
NM_005591.3(MRE11):c.476T>C (p.Val159Ala) rs140130291
NM_005591.3(MRE11):c.49G>A (p.Val17Ile) rs1060501790
NM_005591.3(MRE11):c.49G>C (p.Val17Leu) rs1060501790
NM_005591.3(MRE11):c.508C>A (p.Gln170Lys) rs587782030
NM_005591.3(MRE11):c.526A>G (p.Ile176Val) rs587781676
NM_005591.3(MRE11):c.529G>A (p.Ala177Thr) rs142996063
NM_005591.3(MRE11):c.545-13A>G rs370306271
NM_005591.3(MRE11):c.585T>C (p.Asn195=) rs886048760
NM_005591.3(MRE11):c.59A>G (p.Asp20Gly) rs1565242083
NM_005591.3(MRE11):c.626C>T (p.Ser209Phe) rs1555014479
NM_005591.3(MRE11):c.640T>C (p.Phe214Leu) rs750929369
NM_005591.3(MRE11):c.661A>C (p.Ser221Arg) rs587781272
NM_005591.3(MRE11):c.673A>C (p.Ser225Arg) rs763790530
NM_005591.3(MRE11):c.677C>G (p.Thr226Ser) rs201276188
NM_005591.3(MRE11):c.734A>T (p.His245Leu) rs1555013153
NM_005591.3(MRE11):c.758C>T (p.Pro253Leu) rs587782051
NM_005591.3(MRE11):c.818C>G (p.Ser273Cys) rs143400546
NM_005591.3(MRE11):c.822T>C (p.Leu274=) rs137868143
NM_005591.3(MRE11):c.826C>T (p.Pro276Ser) rs587782742
NM_005591.3(MRE11):c.835G>C (p.Ala279Pro) rs147383852
NM_005591.3(MRE11):c.848A>G (p.His283Arg) rs142727857
NM_005591.3(MRE11):c.863G>A (p.Arg288His) rs190142346
NM_005591.3(MRE11):c.880A>G (p.Met294Val) rs786202636
NM_005591.3(MRE11):c.914G>A (p.Arg305Gln) rs752483206
NM_005591.3(MRE11):c.946A>G (p.Asn316Asp) rs767684060
NM_005591.3(MRE11):c.958A>C (p.Ile320Leu) rs762210984
NM_005591.3(MRE11):c.983T>G (p.Val328Gly) rs587782314

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