ClinVar Miner

List of variants in gene DIS3L2 reported as likely benign for not provided

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Gene type:
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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_152383.5(DIS3L2):c.1426-179G>T rs75750757 0.01383
NM_152383.5(DIS3L2):c.1488T>C (p.His496=) rs72998118 0.01233
NM_152383.5(DIS3L2):c.1125-253C>T rs56128415 0.01232
NM_152383.5(DIS3L2):c.1125-297C>G rs56408197 0.01232
NM_152383.5(DIS3L2):c.1923+99G>A rs115540595 0.01228
NM_152383.5(DIS3L2):c.1924-128C>T rs114469609 0.01226
NM_152383.5(DIS3L2):c.1740-76C>T rs114911246 0.01225
NM_152383.5(DIS3L2):c.1659+86C>T rs77283182 0.01211
NM_152383.5(DIS3L2):c.426C>T (p.Pro142=) rs73001172 0.01166
NM_152383.5(DIS3L2):c.366+250T>G rs72987671 0.01161
NM_152383.5(DIS3L2):c.1740-119T>G rs6733152 0.01151
NM_152383.5(DIS3L2):c.1317+114A>G rs16828707 0.01150
NM_152383.5(DIS3L2):c.1740-77C>T rs148811774 0.01142
NM_152383.5(DIS3L2):c.2394+260G>T rs569682292 0.01097
NM_152383.5(DIS3L2):c.265-15C>A rs114804860 0.01092
NM_152383.5(DIS3L2):c.2394+139G>A rs528703905 0.01080
NM_152383.5(DIS3L2):c.*113T>G rs116379923 0.01035
NM_152383.5(DIS3L2):c.1740-20A>C rs780678383 0.00934
NM_152383.5(DIS3L2):c.2496+239C>T rs9679389 0.00926
NM_152383.5(DIS3L2):c.1125-131C>T rs112239374 0.00725
NM_152383.5(DIS3L2):c.1739+28A>G rs7598306 0.00711
NM_152383.5(DIS3L2):c.1740-11A>C rs762813767 0.00650
NM_152383.5(DIS3L2):c.2394+28G>A rs116284581 0.00647
NM_152383.5(DIS3L2):c.703-299T>C rs115555819 0.00579
NM_152383.5(DIS3L2):c.1740-238C>T rs187858739 0.00576
NM_152383.5(DIS3L2):c.2394+131G>T rs559975255 0.00572
NM_001257281.2(DIS3L2):c.*49A>T rs114614578 0.00522
NM_152383.5(DIS3L2):c.702+10T>G rs184764939 0.00343
NM_152383.5(DIS3L2):c.*13G>A rs200467865 0.00304
NM_152383.5(DIS3L2):c.702+39T>G rs75968600 0.00289
NM_152383.5(DIS3L2):c.2370C>T (p.Gly790=) rs199541622 0.00242
NM_152383.5(DIS3L2):c.1740-7T>C rs1160509197 0.00205
NM_001257281.2(DIS3L2):c.1587C>T (p.Asn529=) rs556095213 0.00121
NM_152383.5(DIS3L2):c.*77G>T rs77517611 0.00113
NM_152383.5(DIS3L2):c.1447C>G (p.Arg483Gly) rs186865544 0.00073
NM_152383.5(DIS3L2):c.263C>T (p.Pro88Leu) rs202059499 0.00073
NM_152383.5(DIS3L2):c.1911A>C (p.Ala637=) rs563679311 0.00072
NM_152383.5(DIS3L2):c.795C>T (p.Tyr265=) rs202042951 0.00047
NM_152383.5(DIS3L2):c.2367C>T (p.Tyr789=) rs770189518 0.00026
NM_152383.5(DIS3L2):c.2424G>A (p.Gln808=) rs369113667 0.00016
NM_152383.5(DIS3L2):c.351C>T (p.Pro117=) rs141249322 0.00013
NM_152383.5(DIS3L2):c.1599C>T (p.His533=) rs760229466 0.00011
NM_152383.5(DIS3L2):c.108G>A (p.Lys36=) rs371477071 0.00010
NM_152383.5(DIS3L2):c.1023C>T (p.Gly341=) rs201122747 0.00008
NM_152383.5(DIS3L2):c.2067C>T (p.Tyr689=) rs186340144 0.00007
NM_001257281.2(DIS3L2):c.1644T>C (p.Asp548=) rs142369101 0.00006
NM_152383.5(DIS3L2):c.1686C>T (p.His562=) rs772512074 0.00005
NM_152383.5(DIS3L2):c.729T>C (p.His243=) rs371095624 0.00004
NM_152383.5(DIS3L2):c.2592C>T (p.Gly864=) rs376585486 0.00003
NM_152383.5(DIS3L2):c.453G>A (p.Pro151=) rs567611268 0.00003
NM_152383.5(DIS3L2):c.1740-5T>C rs1433218863 0.00002
NM_152383.5(DIS3L2):c.2154G>A (p.Ala718=) rs371733417 0.00002
NM_152383.5(DIS3L2):c.519C>T (p.Ser173=) rs143680532 0.00002
NM_152383.5(DIS3L2):c.1116G>A (p.Arg372=) rs755028564 0.00001
NM_152383.5(DIS3L2):c.2049A>G (p.Pro683=) rs757277629 0.00001
NM_152383.5(DIS3L2):c.2052G>A (p.Ala684=) rs529468340 0.00001
NM_152383.5(DIS3L2):c.2079G>T (p.Val693=) rs772840869 0.00001
NM_152383.5(DIS3L2):c.2628C>T (p.Asp876=) rs760111036 0.00001
NM_152383.5(DIS3L2):c.540C>T (p.Gly180=) rs369500890 0.00001
NM_001257281.2(DIS3L2):c.1632C>G (p.Pro544=)
NM_001257281.2(DIS3L2):c.1651_1652insGGG (p.Glu550_Ala551insGly) rs141560952
NM_152383.5(DIS3L2):c.*11CCGCCTGCC[2] rs538186468
NM_152383.5(DIS3L2):c.*314A>T rs187723884
NM_152383.5(DIS3L2):c.2011-135G>A
NM_152383.5(DIS3L2):c.2295T>C (p.Ser765=) rs763103187
NM_152383.5(DIS3L2):c.558G>C (p.Leu186=) rs780991652
NM_152383.5(DIS3L2):c.602-298C>T rs73996906
NM_152383.5(DIS3L2):c.702+45C>G

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