ClinVar Miner

Variants in gene DIS3L2 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 32
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HGVS dbSNP gnomAD frequency
NM_152383.5(DIS3L2):c.265-15C>A rs114804860 0.01092
NM_152383.5(DIS3L2):c.878C>A (p.Pro293His) rs187563594 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.410A>G (p.Tyr137Cys) rs201733073 0.00072
NM_152383.5(DIS3L2):c.1205-13C>T rs116327839 0.00038
NM_152383.5(DIS3L2):c.2424G>A (p.Gln808=) rs369113667 0.00016
NM_152383.5(DIS3L2):c.1203C>T (p.Asp401=) rs370165461 0.00011
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.2124C>T (p.Asp708=) rs368518323 0.00010
NM_152383.5(DIS3L2):c.210+10A>G rs201117797 0.00009
NM_152383.5(DIS3L2):c.1205-12G>A rs779551518 0.00008
NM_152383.5(DIS3L2):c.1908C>T (p.Ser636=) rs778830625 0.00007
NM_152383.5(DIS3L2):c.2067C>T (p.Tyr689=) rs186340144 0.00007
NM_152383.5(DIS3L2):c.1125-6T>G rs764758535 0.00005
NM_152383.5(DIS3L2):c.1158C>T (p.Thr386=) rs539081624 0.00005
NM_152383.5(DIS3L2):c.2159-7T>C rs368022190 0.00005
NM_152383.5(DIS3L2):c.453G>A (p.Pro151=) rs567611268 0.00003
NM_152383.5(DIS3L2):c.2207C>T (p.Ala736Val) rs780625125 0.00002
NM_152383.5(DIS3L2):c.519C>T (p.Ser173=) rs143680532 0.00002
NM_152383.5(DIS3L2):c.1425+13A>G rs565049855 0.00001
NM_152383.5(DIS3L2):c.1809G>A (p.Glu603=) rs748787779 0.00001
NM_152383.5(DIS3L2):c.2151C>T (p.Ala717=) rs747739911 0.00001
NM_152383.5(DIS3L2):c.2394C>T (p.Asn798=) rs773602107 0.00001
NM_152383.5(DIS3L2):c.2637C>T (p.Pro879=) rs376299829 0.00001
NM_001257281.2(DIS3L2):c.1651_1652insGGG (p.Glu550_Ala551insGly) rs141560952
NM_152383.5(DIS3L2):c.1836G>A (p.Pro612=) rs202227137
NM_152383.5(DIS3L2):c.2395-13G>T rs374738789
NM_152383.5(DIS3L2):c.2497-14T>C rs1283433476
NM_152383.5(DIS3L2):c.780A>G (p.Glu260=) rs2106355380
NM_152383.5(DIS3L2):c.951-8A>G rs886055770

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