ClinVar Miner

List of variants in gene DIS3L2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 32
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HGVS dbSNP gnomAD frequency
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_001257281.2(DIS3L2):c.1587C>T (p.Asn529=) rs556095213 0.00121
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.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.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.2295T>C (p.Ser765=) rs763103187
NM_152383.5(DIS3L2):c.558G>C (p.Leu186=) rs780991652
NM_152383.5(DIS3L2):c.702+45C>G

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