ClinVar Miner

List of variants in gene NEBL reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 82
Download table as spreadsheet
HGVS dbSNP
NM_006393.3(NEBL):c.1008+15G>A rs375728589
NM_006393.3(NEBL):c.1008+8C>G rs376842299
NM_006393.3(NEBL):c.120A>G (p.Glu40=) rs397517203
NM_006393.3(NEBL):c.1228-7C>T rs200231082
NM_006393.3(NEBL):c.1269A>G (p.Lys423=) rs138932199
NM_006393.3(NEBL):c.1272A>G (p.Gly424=) rs727504866
NM_006393.3(NEBL):c.1302C>G (p.Ile434Met) rs202112717
NM_006393.3(NEBL):c.1449+14G>A rs373699154
NM_006393.3(NEBL):c.153+15T>G rs397517204
NM_006393.3(NEBL):c.154-11C>A rs41277376
NM_006393.3(NEBL):c.1728T>C (p.Asp576=) rs1528182
NM_006393.3(NEBL):c.1775C>A (p.Ala592Glu) rs146275785
NM_006393.3(NEBL):c.180G>C (p.Lys60Asn) rs41277374
NM_006393.3(NEBL):c.1954A>C (p.Ile652Leu) rs200756166
NM_006393.3(NEBL):c.1962+7A>G rs371630900
NM_006393.3(NEBL):c.1963-13C>T rs727504904
NM_006393.3(NEBL):c.2055+7C>A rs368793318
NM_006393.3(NEBL):c.2148+4T>C rs193163659
NM_006393.3(NEBL):c.2347-9C>T rs750957531
NM_006393.3(NEBL):c.240C>T (p.Ile80=) rs727503337
NM_006393.3(NEBL):c.2445G>A (p.Val815=) rs578252294
NM_006393.3(NEBL):c.2475C>T (p.His825=) rs727503334
NM_006393.3(NEBL):c.2482A>G (p.Ile828Val) rs143930021
NM_006393.3(NEBL):c.2547C>T (p.Gly849=) rs180850975
NM_006393.3(NEBL):c.255T>C (p.Ser85=) rs727504471
NM_006393.3(NEBL):c.2654C>T (p.Ser885Phe) rs143584663
NM_006393.3(NEBL):c.2748G>T (p.Pro916=) rs778128527
NM_006393.3(NEBL):c.2761+15C>T rs760162209
NM_006393.3(NEBL):c.2775C>T (p.Pro925=) rs199887353
NM_006393.3(NEBL):c.2820C>T (p.His940=) rs532565487
NM_006393.3(NEBL):c.2913C>T (p.Asp971=) rs575423101
NM_006393.3(NEBL):c.480+10C>A rs377230358
NM_006393.3(NEBL):c.480+11G>A rs769167750
NM_006393.3(NEBL):c.480+3A>G rs71578983
NM_006393.3(NEBL):c.489T>C (p.Tyr163=) rs141153708
NM_006393.3(NEBL):c.56G>A (p.Gly19Glu) rs727503338
NM_006393.3(NEBL):c.82-4A>G rs368268112
NM_006393.3(NEBL):c.994G>A (p.Val332Ile) rs150518045
NM_213569.2(NEBL):c.204A>T (p.Thr68=) rs563150056
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+71713T>C rs1057521303
NM_213569.2(NEBL):c.357+71797T>C rs1057523090
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+73593T>C rs771142727
NM_213569.2(NEBL):c.358-10254T>G rs1292029849
NM_213569.2(NEBL):c.358-13499C>G rs188529864
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.358-18244A>C rs77445663
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.358-2788T>C rs369297283
NM_213569.2(NEBL):c.358-39591C>T rs369037243
NM_213569.2(NEBL):c.358-39627G>T rs776185255
NM_213569.2(NEBL):c.358-39705A>G rs139610204
NM_213569.2(NEBL):c.358-46779G>A rs375771045
NM_213569.2(NEBL):c.358-55794A>G rs794729077
NM_213569.2(NEBL):c.358-6523G>A rs757626106
NM_213569.2(NEBL):c.358-67839_358-67838del rs1064794541
NM_213569.2(NEBL):c.358-980A>G rs376097780
NM_213569.2(NEBL):c.408C>T (p.Pro136=) rs766216481
NM_213569.2(NEBL):c.423T>C (p.Pro141=) rs749572741
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+4099C>T rs200934881
NM_213569.2(NEBL):c.529+4117G>A rs140803920
NM_213569.2(NEBL):c.529+4165C>T rs780103943
NM_213569.2(NEBL):c.529+4222A>T rs146673676
NM_213569.2(NEBL):c.636+9C>T rs377236750
NM_213569.2(NEBL):c.657C>T (p.Tyr219=) rs202184399
NM_213569.2(NEBL):c.69+15G>T rs377648518
NM_213569.2(NEBL):c.732C>T (p.Asp244=) rs144946187

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.