ClinVar Miner

List of variants in gene DIS3L2 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 74
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HGVS dbSNP gnomAD frequency
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.795C>T (p.Tyr265=) rs202042951 0.00047
NM_152383.5(DIS3L2):c.*22dup rs775740747 0.00044
NM_152383.5(DIS3L2):c.1205-13C>T rs116327839 0.00038
NM_152383.5(DIS3L2):c.-142T>A rs549994066 0.00035
NM_152383.5(DIS3L2):c.*72C>T rs138716319 0.00026
NM_152383.5(DIS3L2):c.*208G>A rs886055775 0.00023
NM_152383.5(DIS3L2):c.*44G>A rs372315218 0.00019
NM_152383.5(DIS3L2):c.*127A>G rs755515971 0.00017
NM_152383.5(DIS3L2):c.-52A>G rs750961522 0.00016
NM_152383.5(DIS3L2):c.2424G>A (p.Gln808=) rs369113667 0.00016
NM_152383.5(DIS3L2):c.*301G>T rs886055778 0.00014
NM_152383.5(DIS3L2):c.2329A>G (p.Ile777Val) rs2697798 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.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.1680G>A (p.Leu560=) rs377644356 0.00008
NM_152383.5(DIS3L2):c.*73G>A rs768428203 0.00007
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.1546A>T (p.Ile516Phe) rs183901077 0.00006
NM_152383.5(DIS3L2):c.1839C>T (p.Pro613=) rs187677159 0.00006
NM_152383.5(DIS3L2):c.674C>T (p.Ser225Leu) rs201453807 0.00006
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.*18C>T rs538449626 0.00004
NM_152383.5(DIS3L2):c.2060G>A (p.Arg687Gln) rs749596505 0.00004
NM_152383.5(DIS3L2):c.1970G>A (p.Arg657His) rs757443947 0.00003
NM_152383.5(DIS3L2):c.305G>C (p.Arg102Pro) rs372013568 0.00003
NM_152383.5(DIS3L2):c.453G>A (p.Pro151=) rs567611268 0.00003
NM_152383.5(DIS3L2):c.1825C>T (p.Arg609Trp) rs370822831 0.00002
NM_152383.5(DIS3L2):c.2207C>T (p.Ala736Val) rs780625125 0.00002
NM_152383.5(DIS3L2):c.2271C>G (p.Phe757Leu) rs560015968 0.00002
NM_152383.5(DIS3L2):c.519C>T (p.Ser173=) rs143680532 0.00002
NM_152383.5(DIS3L2):c.712A>G (p.Ile238Val) rs774656238 0.00002
NM_152383.5(DIS3L2):c.*475G>C rs745474291 0.00001
NM_152383.5(DIS3L2):c.*63C>T rs1332852401 0.00001
NM_152383.5(DIS3L2):c.-102G>A rs535486739 0.00001
NM_152383.5(DIS3L2):c.-67G>A rs886055768 0.00001
NM_152383.5(DIS3L2):c.1188C>T (p.Cys396=) rs145607185 0.00001
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.1856G>A (p.Ser619Asn) rs752063922 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.2635C>G (p.Pro879Ala) rs1246277178 0.00001
NM_152383.5(DIS3L2):c.2637C>T (p.Pro879=) rs376299829 0.00001
NM_152383.5(DIS3L2):c.566G>C (p.Gly189Ala) rs755258805 0.00001
NM_152383.5(DIS3L2):c.821G>A (p.Arg274Gln) rs1482350666 0.00001
NM_152383.5(DIS3L2):c.*111G>A rs886055774
NM_152383.5(DIS3L2):c.*13G>T rs200467865
NM_152383.5(DIS3L2):c.*251C>A rs886055776
NM_152383.5(DIS3L2):c.*301dup rs555818431
NM_152383.5(DIS3L2):c.*361del rs886055779
NM_152383.5(DIS3L2):c.*551_*554dup rs886055780
NM_152383.5(DIS3L2):c.-143C>G rs924366103
NM_152383.5(DIS3L2):c.-58_-54del rs886055769
NM_152383.5(DIS3L2):c.-95C>T rs748871880
NM_152383.5(DIS3L2):c.1337G>C (p.Arg446Thr) rs369290389
NM_152383.5(DIS3L2):c.1534G>A (p.Glu512Lys) rs1693767237
NM_152383.5(DIS3L2):c.1659+6T>A rs1693772966
NM_152383.5(DIS3L2):c.1731G>C (p.Glu577Asp) rs1694818817
NM_152383.5(DIS3L2):c.1829A>G (p.His610Arg) rs1575023333
NM_152383.5(DIS3L2):c.1836G>A (p.Pro612=) rs202227137
NM_152383.5(DIS3L2):c.2051C>T (p.Ala684Val) rs781674022
NM_152383.5(DIS3L2):c.2080C>T (p.Pro694Ser) rs886055771
NM_152383.5(DIS3L2):c.221G>A (p.Arg74Lys) rs893912059
NM_152383.5(DIS3L2):c.2497-14T>C rs1283433476
NM_152383.5(DIS3L2):c.47C>A (p.Pro16His) rs769111524
NM_152383.5(DIS3L2):c.613G>A (p.Gly205Ser) rs1698187916
NM_152383.5(DIS3L2):c.951-8A>G rs886055770

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