ClinVar Miner

List of variants in gene NEBL reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 89
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HGVS dbSNP
NM_213569.2(NEBL):c.250-214A>G
NM_213569.2(NEBL):c.250-215T>G
NM_213569.2(NEBL):c.357+64417G>T rs1426428551
NM_213569.2(NEBL):c.357+64447A>G rs766280453
NM_213569.2(NEBL):c.357+64458A>G rs772236141
NM_213569.2(NEBL):c.357+64514A>G rs967421212
NM_213569.2(NEBL):c.357+64535T>C rs746405718
NM_213569.2(NEBL):c.357+64639A>G rs368268112
NM_213569.2(NEBL):c.357+71569T>C
NM_213569.2(NEBL):c.357+71713T>C rs1057521303
NM_213569.2(NEBL):c.357+71749G>C rs41277374
NM_213569.2(NEBL):c.357+71797T>C rs1057523090
NM_213569.2(NEBL):c.357+71809C>T rs727503337
NM_213569.2(NEBL):c.357+72010A>C
NM_213569.2(NEBL):c.357+73444_357+73450delinsCCTGG rs1554799332
NM_213569.2(NEBL):c.357+73482C>T rs1256058724
NM_213569.2(NEBL):c.357+73483A>G rs762884881
NM_213569.2(NEBL):c.357+73500T>A
NM_213569.2(NEBL):c.357+73593T>C rs771142727
NM_213569.2(NEBL):c.357T>C (p.Asn119=) rs115708584
NM_213569.2(NEBL):c.358-10018G>A
NM_213569.2(NEBL):c.358-10254T>G rs1292029849
NM_213569.2(NEBL):c.358-10276A>C rs200756166
NM_213569.2(NEBL):c.358-13499C>G rs188529864
NM_213569.2(NEBL):c.358-1410G>A
NM_213569.2(NEBL):c.358-15572C>G rs373474665
NM_213569.2(NEBL):c.358-15575C>G rs373748632
NM_213569.2(NEBL):c.358-15591C>T rs146275785
NM_213569.2(NEBL):c.358-17968T>C
NM_213569.2(NEBL):c.358-18152A>G
NM_213569.2(NEBL):c.358-18244A>C rs77445663
NM_213569.2(NEBL):c.358-18458C>T
NM_213569.2(NEBL):c.358-22383A>G
NM_213569.2(NEBL):c.358-22703T>C rs370957821
NM_213569.2(NEBL):c.358-2668A>G rs368494211
NM_213569.2(NEBL):c.358-27826A>G rs901799820
NM_213569.2(NEBL):c.358-27835C>G rs202112717
NM_213569.2(NEBL):c.358-2788T>C rs369297283
NM_213569.2(NEBL):c.358-39529C>T
NM_213569.2(NEBL):c.358-39590G>A rs375728589
NM_213569.2(NEBL):c.358-39591C>T rs369037243
NM_213569.2(NEBL):c.358-39597C>G rs376842299
NM_213569.2(NEBL):c.358-39619G>A rs150518045
NM_213569.2(NEBL):c.358-39627G>T rs776185255
NM_213569.2(NEBL):c.358-39705A>G rs139610204
NM_213569.2(NEBL):c.358-4451A>G
NM_213569.2(NEBL):c.358-45040C>T
NM_213569.2(NEBL):c.358-45274G>A
NM_213569.2(NEBL):c.358-45656A>G
NM_213569.2(NEBL):c.358-4656T>C rs193163659
NM_213569.2(NEBL):c.358-46779G>A rs375771045
NM_213569.2(NEBL):c.358-46851G>A
NM_213569.2(NEBL):c.358-47191T>A
NM_213569.2(NEBL):c.358-55794A>G rs794729077
NM_213569.2(NEBL):c.358-56629G>T
NM_213569.2(NEBL):c.358-56893T>C rs141153708
NM_213569.2(NEBL):c.358-57058A>C
NM_213569.2(NEBL):c.358-6477C>A rs368793318
NM_213569.2(NEBL):c.358-6523G>A rs757626106
NM_213569.2(NEBL):c.358-6589C>T rs727504904
NM_213569.2(NEBL):c.358-67839_358-67838del rs1064794541
NM_213569.2(NEBL):c.358-67843G>A rs769167750
NM_213569.2(NEBL):c.358-67844C>A rs377230358
NM_213569.2(NEBL):c.358-67851A>G rs71578983
NM_213569.2(NEBL):c.358-68192A>G
NM_213569.2(NEBL):c.358-980A>G rs376097780
NM_213569.2(NEBL):c.358-9C>T rs750957531
NM_213569.2(NEBL):c.408C>T (p.Pro136=) rs766216481
NM_213569.2(NEBL):c.417C>T (p.Asp139=)
NM_213569.2(NEBL):c.423T>C (p.Pro141=) rs749572741
NM_213569.2(NEBL):c.493A>G (p.Ile165Val) rs143930021
NM_213569.2(NEBL):c.495C>T (p.Ile165=) rs1315850585
NM_213569.2(NEBL):c.529+10C>T rs747607700
NM_213569.2(NEBL):c.529+14G>A rs551568597
NM_213569.2(NEBL):c.529+20C>T rs755901579
NM_213569.2(NEBL):c.529+3050del
NM_213569.2(NEBL):c.529+4099C>T rs200934881
NM_213569.2(NEBL):c.529+4117G>A rs140803920
NM_213569.2(NEBL):c.529+4152C>T rs143584663
NM_213569.2(NEBL):c.529+4165C>T rs780103943
NM_213569.2(NEBL):c.529+4222A>T rs146673676
NM_213569.2(NEBL):c.529+4274C>T rs760162209
NM_213569.2(NEBL):c.529+4539T>A
NM_213569.2(NEBL):c.530-263T>A
NM_213569.2(NEBL):c.530-64T>A
NM_213569.2(NEBL):c.543C>T (p.Pro181=) rs199887353
NM_213569.2(NEBL):c.636+9C>T rs377236750
NM_213569.2(NEBL):c.657C>T (p.Tyr219=) rs202184399
NM_213569.2(NEBL):c.732C>T (p.Asp244=) rs144946187

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