ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP
NM_152383.4(DIS3L2):c.*111G>A rs886055774
NM_152383.4(DIS3L2):c.*127A>G rs755515971
NM_152383.4(DIS3L2):c.*208G>A rs886055775
NM_152383.4(DIS3L2):c.*22dupG rs775740747
NM_152383.4(DIS3L2):c.*251C>A rs886055776
NM_152383.4(DIS3L2):c.*301G>T rs886055778
NM_152383.4(DIS3L2):c.*301dupG rs555818431
NM_152383.4(DIS3L2):c.*361delG rs886055779
NM_152383.4(DIS3L2):c.*551_*554dupATTA rs886055780
NM_152383.4(DIS3L2):c.*558T>C rs143549263
NM_152383.4(DIS3L2):c.-102G>A rs535486739
NM_152383.4(DIS3L2):c.-142T>A rs549994066
NM_152383.4(DIS3L2):c.-229C>T rs886055767
NM_152383.4(DIS3L2):c.-250C>G rs769255550
NM_152383.4(DIS3L2):c.-52A>G rs750961522
NM_152383.4(DIS3L2):c.-58_-54delGAGCT rs886055769
NM_152383.4(DIS3L2):c.-67G>A rs886055768
NM_152383.4(DIS3L2):c.1158C>T (p.Thr386=) rs539081624
NM_152383.4(DIS3L2):c.1317+15C>G rs553691050
NM_152383.4(DIS3L2):c.1425+13A>G rs565049855
NM_152383.4(DIS3L2):c.1599C>T (p.His533=) rs760229466
NM_152383.4(DIS3L2):c.1680G>A (p.Leu560=) rs377644356
NM_152383.4(DIS3L2):c.1809G>A (p.Glu603=) rs748787779
NM_152383.4(DIS3L2):c.1908C>T (p.Ser636=) rs778830625
NM_152383.4(DIS3L2):c.2060G>A (p.Arg687Gln) rs749596505
NM_152383.4(DIS3L2):c.2067C>T (p.Tyr689=) rs186340144
NM_152383.4(DIS3L2):c.2080C>T (p.Pro694Ser) rs886055771
NM_152383.4(DIS3L2):c.2124C>T (p.Asp708=) rs368518323
NM_152383.4(DIS3L2):c.2151C>T (p.Ala717=) rs747739911
NM_152383.4(DIS3L2):c.2207C>T (p.Ala736Val) rs780625125
NM_152383.4(DIS3L2):c.2424G>A (p.Gln808=) rs369113667
NM_152383.4(DIS3L2):c.2637C>T (p.Pro879=) rs376299829
NM_152383.4(DIS3L2):c.263C>T (p.Pro88Leu) rs202059499
NM_152383.4(DIS3L2):c.410A>G (p.Tyr137Cys) rs201733073
NM_152383.4(DIS3L2):c.519C>T (p.Ser173=) rs143680532
NM_152383.4(DIS3L2):c.674C>T (p.Ser225Leu) rs201453807
NM_152383.4(DIS3L2):c.702+10T>G rs184764939
NM_152383.4(DIS3L2):c.712A>G (p.Ile238Val) rs774656238
NM_152383.4(DIS3L2):c.795C>T (p.Tyr265=) rs202042951
NM_152383.4(DIS3L2):c.951-8A>G rs886055770

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