ClinVar Miner

List of variants in gene NEBL reported as benign

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Gene type:
ClinVar version:
Total variants: 93
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HGVS dbSNP
GRCh38/hg38 10p12.31(chr10:20906254-20910631)x1
NC_000010.11:g.20787587del
NC_000010.11:g.20852512del
NM_213569.2(NEBL):c.*4T>A rs727504947
NM_213569.2(NEBL):c.-7C>T rs141707642
NM_213569.2(NEBL):c.164+80C>T
NM_213569.2(NEBL):c.357+285A>G
NM_213569.2(NEBL):c.357+63739C>T
NM_213569.2(NEBL):c.357+63863C>T
NM_213569.2(NEBL):c.357+64420C>T rs368463931
NM_213569.2(NEBL):c.357+64477C>T rs114918858
NM_213569.2(NEBL):c.357+64493A>C rs536400111
NM_213569.2(NEBL):c.357+64670T>C rs140734883
NM_213569.2(NEBL):c.357+64681A>G rs397517203
NM_213569.2(NEBL):c.357+64729T>G rs397517204
NM_213569.2(NEBL):c.357+64780T>G
NM_213569.2(NEBL):c.357+64940C>T
NM_213569.2(NEBL):c.357+71441T>A
NM_213569.2(NEBL):c.357+71674A>T
NM_213569.2(NEBL):c.357+71712C>A rs41277376
NM_213569.2(NEBL):c.357+71749G>C rs41277374
NM_213569.2(NEBL):c.357+71760A>G rs71578975
NM_213569.2(NEBL):c.357+72027C>T
NM_213569.2(NEBL):c.357+72071T>C
NM_213569.2(NEBL):c.357+73449dup rs57918610
NM_213569.2(NEBL):c.357+73457del rs57918610
NM_213569.2(NEBL):c.357+73473C>G rs147622517
NM_213569.2(NEBL):c.357+73656C>T
NM_213569.2(NEBL):c.357+73841G>A
NM_213569.2(NEBL):c.357T>C (p.Asn119=) rs115708584
NM_213569.2(NEBL):c.358-10055T>C
NM_213569.2(NEBL):c.358-10242T>A
NM_213569.2(NEBL):c.358-10261A>G rs371630900
NM_213569.2(NEBL):c.358-10268T>A rs4748728
NM_213569.2(NEBL):c.358-1038T>C rs144815863
NM_213569.2(NEBL):c.358-13463A>G
NM_213569.2(NEBL):c.358-13499C>G rs188529864
NM_213569.2(NEBL):c.358-13515A>G rs79718972
NM_213569.2(NEBL):c.358-13539C>A rs146471913
NM_213569.2(NEBL):c.358-13739T>G
NM_213569.2(NEBL):c.358-1405G>T
NM_213569.2(NEBL):c.358-15638T>C rs1528182
NM_213569.2(NEBL):c.358-18247T>C rs10491056
NM_213569.2(NEBL):c.358-18652T>G rs45628140
NM_213569.2(NEBL):c.358-22559G>A rs373699154
NM_213569.2(NEBL):c.358-2744A>G rs71535732
NM_213569.2(NEBL):c.358-27719A>G
NM_213569.2(NEBL):c.358-2782G>A rs71578956
NM_213569.2(NEBL):c.358-28012G>T
NM_213569.2(NEBL):c.358-2825T>A
NM_213569.2(NEBL):c.358-2963C>T
NM_213569.2(NEBL):c.358-32413G>C rs41277370
NM_213569.2(NEBL):c.358-32434T>G rs71578938
NM_213569.2(NEBL):c.358-37463C>A rs146198369
NM_213569.2(NEBL):c.358-37520A>G rs4025981
NM_213569.2(NEBL):c.358-37659C>T
NM_213569.2(NEBL):c.358-37814T>A
NM_213569.2(NEBL):c.358-39587C>T rs75903914
NM_213569.2(NEBL):c.358-39600A>G rs703089
NM_213569.2(NEBL):c.358-39601C>T rs71534253
NM_213569.2(NEBL):c.358-39620C>T
NM_213569.2(NEBL):c.358-39983G>C
NM_213569.2(NEBL):c.358-45501A>T
NM_213569.2(NEBL):c.358-45549C>T
NM_213569.2(NEBL):c.358-45651A>G
NM_213569.2(NEBL):c.358-45742T>G
NM_213569.2(NEBL):c.358-46536G>T
NM_213569.2(NEBL):c.358-46715G>T
NM_213569.2(NEBL):c.358-47146G>C
NM_213569.2(NEBL):c.358-4751T>C rs74120667
NM_213569.2(NEBL):c.358-55623A>G
NM_213569.2(NEBL):c.358-55752C>A rs2296610
NM_213569.2(NEBL):c.358-55784C>T rs111854914
NM_213569.2(NEBL):c.358-56791T>C rs185873503
NM_213569.2(NEBL):c.358-6378G>A
NM_213569.2(NEBL):c.358-6485C>T rs146218038
NM_213569.2(NEBL):c.358-6508G>A rs1006363
NM_213569.2(NEBL):c.358-67851A>G rs71578983
NM_213569.2(NEBL):c.358-6837A>G
NM_213569.2(NEBL):c.358-993G>A rs201822024
NM_213569.2(NEBL):c.493A>G (p.Ile165Val) rs143930021
NM_213569.2(NEBL):c.529+2662G>T
NM_213569.2(NEBL):c.529+275A>G
NM_213569.2(NEBL):c.529+2869del
NM_213569.2(NEBL):c.529+3929T>C
NM_213569.2(NEBL):c.529+4183C>T rs140245727
NM_213569.2(NEBL):c.529+4486C>G
NM_213569.2(NEBL):c.529+4577C>T
NM_213569.2(NEBL):c.530-70G>A
NM_213569.2(NEBL):c.588C>T (p.His196=) rs532565487
NM_213569.2(NEBL):c.636+31G>T
NM_213569.2(NEBL):c.637-232C>G
NM_213569.2(NEBL):c.765A>G (p.Thr255=) rs2296614

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