ClinVar Miner

List of variants in gene DIS3L2 reported as uncertain significance for not provided

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_152383.5(DIS3L2):c.265-15C>A rs114804860 0.01092
NM_152383.5(DIS3L2):c.1447C>G (p.Arg483Gly) rs186865544 0.00073
NM_152383.5(DIS3L2):c.410A>G (p.Tyr137Cys) rs201733073 0.00072
NM_152383.5(DIS3L2):c.662C>G (p.Thr221Arg) rs201020526 0.00052
NM_152383.5(DIS3L2):c.1722G>T (p.Glu574Asp) rs191608083 0.00041
NM_152383.5(DIS3L2):c.301G>T (p.Ala101Ser) rs199857926 0.00028
NM_152383.5(DIS3L2):c.2409G>T (p.Arg803=) rs148106618 0.00014
NM_152383.5(DIS3L2):c.1727G>A (p.Arg576His) rs200386096 0.00011
NM_152383.5(DIS3L2):c.1300G>A (p.Val434Ile) rs758366698 0.00005
NM_152383.5(DIS3L2):c.2362C>T (p.Arg788Cys) rs777778396 0.00004
NM_152383.5(DIS3L2):c.1564A>G (p.Ser522Gly) rs199980393 0.00003
NM_152383.5(DIS3L2):c.2227C>T (p.Arg743Cys) rs765865656 0.00003
NM_152383.5(DIS3L2):c.1483G>A (p.Glu495Lys) rs376140965 0.00002
NM_152383.5(DIS3L2):c.1826G>A (p.Arg609Gln) rs774228906 0.00002
NM_001257281.2(DIS3L2):c.1625dup (p.His542fs) rs757880754 0.00001
NM_152383.5(DIS3L2):c.1862T>C (p.Leu621Pro) rs772312903 0.00001
NM_152383.5(DIS3L2):c.2210A>G (p.Asp737Gly) rs769764733 0.00001
NM_152383.5(DIS3L2):c.2585C>T (p.Thr862Ile) rs778725551 0.00001
NM_152383.5(DIS3L2):c.695C>T (p.Ser232Leu) rs747734015 0.00001
NM_001257281.2(DIS3L2):c.1651_1652insGGG (p.Glu550_Ala551insGly) rs141560952
NM_152383.5(DIS3L2):c.1112G>T (p.Arg371Ile) rs753830826
NM_152383.5(DIS3L2):c.1253C>T (p.Pro418Leu) rs752820747
NM_152383.5(DIS3L2):c.136A>G (p.Lys46Glu) rs756293168
NM_152383.5(DIS3L2):c.1858G>A (p.Asp620Asn) rs2106348116
NM_152383.5(DIS3L2):c.2263A>G (p.Ser755Gly) rs1281916376
NM_152383.5(DIS3L2):c.2496+1G>T rs1559220985
NM_152383.5(DIS3L2):c.2540A>G (p.Glu847Gly) rs1695954431
NM_152383.5(DIS3L2):c.313G>T (p.Ala105Ser) rs1694761855
NM_152383.5(DIS3L2):c.33_34delinsAA (p.Pro12Thr) rs1559542257
NM_152383.5(DIS3L2):c.796G>T (p.Ala266Ser) rs772470899

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