ClinVar Miner

List of variants in gene DIS3L2 reported as likely benign for Renal hamartomas nephroblastomatosis and fetal gigantism

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Gene type:
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Total variants: 115
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HGVS dbSNP
NM_152383.4(DIS3L2):c.*103A>G rs113002914
NM_152383.4(DIS3L2):c.*13G>A rs200467865
NM_152383.4(DIS3L2):c.*255C>T rs143054885
NM_152383.4(DIS3L2):c.*86del rs373401005
NM_152383.4(DIS3L2):c.1011A>G (p.Leu337=) rs1553612378
NM_152383.4(DIS3L2):c.1023C>T (p.Gly341=) rs201122747
NM_152383.4(DIS3L2):c.102C>T (p.Asp34=) rs764957786
NM_152383.4(DIS3L2):c.1056A>G (p.Leu352=) rs1286895716
NM_152383.4(DIS3L2):c.108G>A (p.Lys36=) rs371477071
NM_152383.4(DIS3L2):c.1124+8C>T rs778977139
NM_152383.4(DIS3L2):c.1125-10T>C rs1553536952
NM_152383.4(DIS3L2):c.1131C>T (p.Asp377=) rs1021555252
NM_152383.4(DIS3L2):c.1158C>T (p.Thr386=) rs539081624
NM_152383.4(DIS3L2):c.1170C>T (p.Leu390=) rs17272089
NM_152383.4(DIS3L2):c.1203C>T (p.Asp401=) rs370165461
NM_152383.4(DIS3L2):c.1236C>T (p.Asp412=) rs765535316
NM_152383.4(DIS3L2):c.1278G>A (p.Val426=) rs1488275564
NM_152383.4(DIS3L2):c.1290G>A (p.Arg430=) rs779790592
NM_152383.4(DIS3L2):c.1308G>A (p.Leu436=) rs369878019
NM_152383.4(DIS3L2):c.1317+7A>G rs747640827
NM_152383.4(DIS3L2):c.1377C>T (p.Ser459=) rs376722215
NM_152383.4(DIS3L2):c.1398G>C (p.Val466=) rs762018625
NM_152383.4(DIS3L2):c.1448G>A (p.Arg483Gln) rs148474013
NM_152383.4(DIS3L2):c.1488T>C (p.His496=) rs72998118
NM_152383.4(DIS3L2):c.1570G>A (p.Glu524Lys) rs201308521
NM_152383.4(DIS3L2):c.1584C>T (p.Ala528=) rs769018996
NM_152383.4(DIS3L2):c.1599C>T (p.His533=) rs760229466
NM_152383.4(DIS3L2):c.1638C>T (p.Asp546=) rs775532734
NM_152383.4(DIS3L2):c.1660-7T>C rs1553546465
NM_152383.4(DIS3L2):c.1660-8C>G rs373987145
NM_152383.4(DIS3L2):c.1686C>T (p.His562=) rs772512074
NM_152383.4(DIS3L2):c.1707A>G (p.Gly569=) rs776261138
NM_152383.4(DIS3L2):c.1737C>T (p.Asn579=) rs370101007
NM_152383.4(DIS3L2):c.1739+10T>C rs1060504802
NM_152383.4(DIS3L2):c.1739+9C>T rs1060504801
NM_152383.4(DIS3L2):c.1752G>A (p.Glu584=) rs1375650718
NM_152383.4(DIS3L2):c.1782C>G (p.Ala594=) rs765160562
NM_152383.4(DIS3L2):c.1797C>T (p.Arg599=) rs757523875
NM_152383.4(DIS3L2):c.1800C>A (p.Ala600=) rs374119466
NM_152383.4(DIS3L2):c.1800C>T (p.Ala600=) rs374119466
NM_152383.4(DIS3L2):c.1806C>T (p.Pro602=) rs755655199
NM_152383.4(DIS3L2):c.1809G>A (p.Glu603=) rs748787779
NM_152383.4(DIS3L2):c.1833C>A (p.Pro611=) rs747955751
NM_152383.4(DIS3L2):c.1836G>A (p.Pro612=) rs202227137
NM_152383.4(DIS3L2):c.1836G>C (p.Pro612=) rs202227137
NM_152383.4(DIS3L2):c.1836G>T (p.Pro612=) rs202227137
NM_152383.4(DIS3L2):c.1911A>G (p.Ala637=) rs563679311
NM_152383.4(DIS3L2):c.1932G>C (p.Leu644=) rs1553550908
NM_152383.4(DIS3L2):c.1935C>A (p.Thr645=) rs754195941
NM_152383.4(DIS3L2):c.1935C>T (p.Thr645=) rs754195941
NM_152383.4(DIS3L2):c.1977G>A (p.Glu659=) rs1553550932
NM_152383.4(DIS3L2):c.2010+10G>T rs771412088
NM_152383.4(DIS3L2):c.2010+8G>A rs202229172
NM_152383.4(DIS3L2):c.2011-9G>A rs773963007
NM_152383.4(DIS3L2):c.2040G>T (p.Leu680=) rs751823544
NM_152383.4(DIS3L2):c.2067C>T (p.Tyr689=) rs186340144
NM_152383.4(DIS3L2):c.2070G>A (p.Ala690=) rs761434540
NM_152383.4(DIS3L2):c.2073C>T (p.Leu691=) rs1413182287
NM_152383.4(DIS3L2):c.2079G>T (p.Val693=) rs772840869
NM_152383.4(DIS3L2):c.210+10A>G rs201117797
NM_152383.4(DIS3L2):c.211-9del rs752596889
NM_152383.4(DIS3L2):c.2124C>T (p.Asp708=) rs368518323
NM_152383.4(DIS3L2):c.2154G>A (p.Ala718=) rs371733417
NM_152383.4(DIS3L2):c.2159-7T>C rs368022190
NM_152383.4(DIS3L2):c.2163T>C (p.Tyr721=) rs376478058
NM_152383.4(DIS3L2):c.2187C>T (p.Pro729=) rs75782436
NM_152383.4(DIS3L2):c.2205G>A (p.Gln735=) rs549582540
NM_152383.4(DIS3L2):c.2208G>A (p.Ala736=) rs745361985
NM_152383.4(DIS3L2):c.2235G>A (p.Ala745=) rs751938833
NM_152383.4(DIS3L2):c.2244C>T (p.Arg748=) rs745415974
NM_152383.4(DIS3L2):c.2253G>A (p.Glu751=) rs896293028
NM_152383.4(DIS3L2):c.2277T>C (p.Ala759=) rs2678530
NM_152383.4(DIS3L2):c.2295T>C (p.Ser765=) rs763103187
NM_152383.4(DIS3L2):c.2349C>T (p.Asp783=) rs377740097
NM_152383.4(DIS3L2):c.2367C>T (p.Tyr789=) rs770189518
NM_152383.4(DIS3L2):c.237G>A (p.Lys79=) rs373861286
NM_152383.4(DIS3L2):c.2394+7G>A rs372069869
NM_152383.4(DIS3L2):c.2394+9C>T rs766054545
NM_152383.4(DIS3L2):c.2404C>T (p.Leu802=) rs1553552076
NM_152383.4(DIS3L2):c.2409G>T (p.Arg803=) rs148106618
NM_152383.4(DIS3L2):c.2424G>A (p.Gln808=) rs369113667
NM_152383.4(DIS3L2):c.2436G>A (p.Lys812=) rs878855225
NM_152383.4(DIS3L2):c.2496+10C>T rs1553552123
NM_152383.4(DIS3L2):c.2559C>T (p.Tyr853=) rs764331420
NM_152383.4(DIS3L2):c.2592C>T (p.Gly864=) rs376585486
NM_152383.4(DIS3L2):c.2628C>T (p.Asp876=) rs760111036
NM_152383.4(DIS3L2):c.2637C>T (p.Pro879=) rs376299829
NM_152383.4(DIS3L2):c.264+9A>C rs745443608
NM_152383.4(DIS3L2):c.264+9A>T rs745443608
NM_152383.4(DIS3L2):c.265-15C>A rs114804860
NM_152383.4(DIS3L2):c.309T>C (p.Asn103=) rs774819151
NM_152383.4(DIS3L2):c.336C>T (p.Val112=) rs755653632
NM_152383.4(DIS3L2):c.34C>T (p.Pro12Ser) rs723044
NM_152383.4(DIS3L2):c.351C>T (p.Pro117=) rs141249322
NM_152383.4(DIS3L2):c.366+9A>T rs878855226
NM_152383.4(DIS3L2):c.405T>C (p.Ala135=) rs1553606112
NM_152383.4(DIS3L2):c.408G>A (p.Ala136=) rs149344471
NM_152383.4(DIS3L2):c.414A>G (p.Glu138=) rs1553606113
NM_152383.4(DIS3L2):c.426C>T (p.Pro142=) rs73001172
NM_152383.4(DIS3L2):c.453G>A (p.Pro151=) rs567611268
NM_152383.4(DIS3L2):c.456A>G (p.Gln152=) rs11887184
NM_152383.4(DIS3L2):c.519C>T (p.Ser173=) rs143680532
NM_152383.4(DIS3L2):c.558G>C (p.Leu186=) rs780991652
NM_152383.4(DIS3L2):c.642C>G (p.Thr214=) rs1055806361
NM_152383.4(DIS3L2):c.675G>A (p.Ser225=) rs756569370
NM_152383.4(DIS3L2):c.702+4A>G rs1057445
NM_152383.4(DIS3L2):c.703-9T>C rs1451942425
NM_152383.4(DIS3L2):c.723A>G (p.Lys241=) rs1553610349
NM_152383.4(DIS3L2):c.738A>G (p.Ala246=) rs781622806
NM_152383.4(DIS3L2):c.781C>T (p.Leu261=) rs1553610364
NM_152383.4(DIS3L2):c.783G>A (p.Leu261=) rs367638559
NM_152383.4(DIS3L2):c.795C>T (p.Tyr265=) rs202042951
NM_152383.4(DIS3L2):c.878C>A (p.Pro293His) rs187563594
NM_152383.4(DIS3L2):c.963G>A (p.Lys321=) rs368863176
NM_152383.4(DIS3L2):c.981T>C (p.Gly327=) rs372569875

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