ClinVar Miner

List of variants in gene NEBL reported as benign by Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine

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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_213569.2(NEBL):c.-7C>T rs141707642
NM_213569.2(NEBL):c.357+64477C>T rs114918858
NM_213569.2(NEBL):c.357+64670T>C rs140734883
NM_213569.2(NEBL):c.357+71760A>G rs71578975
NM_213569.2(NEBL):c.357+73449dup rs57918610
NM_213569.2(NEBL):c.357+73457del rs57918610
NM_213569.2(NEBL):c.357T>C (p.Asn119=) rs115708584
NM_213569.2(NEBL):c.358-10268T>A rs4748728
NM_213569.2(NEBL):c.358-13515A>G rs79718972
NM_213569.2(NEBL):c.358-18247T>C rs10491056
NM_213569.2(NEBL):c.358-18652T>G rs45628140
NM_213569.2(NEBL):c.358-2744A>G rs71535732
NM_213569.2(NEBL):c.358-2782G>A rs71578956
NM_213569.2(NEBL):c.358-32413G>C rs41277370
NM_213569.2(NEBL):c.358-32434T>G rs71578938
NM_213569.2(NEBL):c.358-37520A>G rs4025981
NM_213569.2(NEBL):c.358-39600A>G rs703089
NM_213569.2(NEBL):c.358-39601C>T rs71534253
NM_213569.2(NEBL):c.358-4751T>C rs74120667
NM_213569.2(NEBL):c.358-55752C>A rs2296610
NM_213569.2(NEBL):c.358-55784C>T rs111854914
NM_213569.2(NEBL):c.358-6485C>T rs146218038
NM_213569.2(NEBL):c.358-6508G>A rs1006363
NM_213569.2(NEBL):c.529+4183C>T rs140245727
NM_213569.2(NEBL):c.765A>G (p.Thr255=) rs2296614

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