ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_006393.3(NEBL):c.1051A>G (p.Met351Val) rs4025981 0.05741
NM_006393.3(NEBL):c.1962T>A (p.Asn654Lys) rs4748728 0.05648
NM_006393.3(NEBL):c.1132G>C (p.Asp378His) rs41277370 0.05503
NM_006393.3(NEBL):c.656C>A (p.Ala219Asp) rs2296610 0.01104
NM_006393.3(NEBL):c.2182A>G (p.Thr728Ala) rs71535732 0.00843
NM_006393.3(NEBL):c.191A>G (p.Lys64Arg) rs71578975 0.00786
NM_006393.3(NEBL):c.1861A>G (p.Ile621Val) rs79718972 0.00532
NM_006393.3(NEBL):c.11C>T (p.Pro4Leu) rs114918858 0.00501
NM_006393.3(NEBL):c.180G>C (p.Lys60Asn) rs41277374 0.00382
NM_006393.3(NEBL):c.480+3A>G rs71578983 0.00336
NM_006393.3(NEBL):c.154-11C>A rs41277376 0.00252
NM_006393.3(NEBL):c.2654C>T (p.Ser885Phe) rs143584663 0.00245
NM_006393.3(NEBL):c.1869+8C>G rs188529864 0.00188
NM_006393.3(NEBL):c.2482A>G (p.Ile828Val) rs143930021 0.00132
NM_006393.3(NEBL):c.994G>A (p.Val332Ile) rs150518045 0.00065
NM_006393.3(NEBL):c.1008+8C>G rs376842299 0.00054
NM_006393.3(NEBL):c.1962+7A>G rs371630900 0.00036
NM_006393.3(NEBL):c.1449+14G>A rs373699154 0.00022
NM_006393.3(NEBL):c.82-4A>G rs368268112 0.00021
NM_006393.3(NEBL):c.2417C>T (p.Thr806Ile) rs200705273 0.00020
NM_006393.3(NEBL):c.1728T>C (p.Asp576=) rs1528182 0.00019
NM_006393.3(NEBL):c.1302C>G (p.Ile434Met) rs202112717 0.00016
NM_006393.3(NEBL):c.258+1G>A rs139581346 0.00016
NM_006393.3(NEBL):c.2775C>T (p.Pro925=) rs199887353 0.00016
NM_006393.3(NEBL):c.240C>T (p.Ile80=) rs727503337 0.00014
NM_006393.3(NEBL):c.2868+9C>T rs377236750 0.00014
NM_006393.3(NEBL):c.480+11G>A rs769167750 0.00014
NM_006393.3(NEBL):c.489T>C (p.Tyr163=) rs141153708 0.00014
NM_006393.3(NEBL):c.1008+14C>T rs369037243 0.00012
NM_213569.2(NEBL):c.69+15G>T rs377648518 0.00011
NM_213569.2(NEBL):c.165-6C>G rs201869237 0.00010
NM_006393.3(NEBL):c.120A>G (p.Glu40=) rs397517203 0.00009
NM_006393.3(NEBL):c.2612-11C>T rs200934881 0.00008
NM_213569.2(NEBL):c.204A>T (p.Thr68=) rs563150056 0.00008
NM_006393.3(NEBL):c.1272A>G (p.Gly424=) rs727504866 0.00006
NM_006393.3(NEBL):c.1339-20T>C rs370957821 0.00006
NM_006393.3(NEBL):c.1776+15C>G rs373748632 0.00006
NM_006393.3(NEBL):c.2619G>A (p.Ala873=) rs140803920 0.00006
NM_006393.3(NEBL):c.56G>A (p.Gly19Glu) rs727503338 0.00006
NM_006393.3(NEBL):c.1671+12A>C rs77445663 0.00005
NM_006393.3(NEBL):c.2346+19A>G rs376097780 0.00005
NM_006393.3(NEBL):c.2761+15C>T rs760162209 0.00005
NM_006393.3(NEBL):c.792G>A (p.Ala264=) rs375771045 0.00005
NM_006393.3(NEBL):c.1008+15G>A rs375728589 0.00004
NM_006393.3(NEBL):c.2347-9C>T rs750957531 0.00004
NM_006393.3(NEBL):c.2445G>A (p.Val815=) rs578252294 0.00004
NM_006393.3(NEBL):c.2518+14G>A rs551568597 0.00004
NM_006393.3(NEBL):c.625G>A (p.Ala209Thr) rs142138590 0.00004
NM_006393.3(NEBL):c.-50G>T rs1426428551 0.00003
NM_006393.3(NEBL):c.153+15T>G rs397517204 0.00003
NM_006393.3(NEBL):c.1776+18C>G rs373474665 0.00003
NM_006393.3(NEBL):c.1954A>C (p.Ile652Leu) rs200756166 0.00003
NM_006393.3(NEBL):c.2518+20C>T rs755901579 0.00003
NM_006393.3(NEBL):c.2667C>T (p.Phe889=) rs780103943 0.00003
NM_006393.3(NEBL):c.48A>G (p.Glu16=) rs967421212 0.00003
NM_006393.3(NEBL):c.1963-13C>T rs727504904 0.00002
NM_006393.3(NEBL):c.2397C>T (p.Pro799=) rs766216481 0.00002
NM_006393.3(NEBL):c.2412T>C (p.Pro804=) rs749572741 0.00002
NM_006393.3(NEBL):c.1228-7C>T rs200231082 0.00001
NM_006393.3(NEBL):c.2016G>A (p.Glu672=) rs757626106 0.00001
NM_006393.3(NEBL):c.2241+17A>G rs368494211 0.00001
NM_006393.3(NEBL):c.2518+10C>T rs747607700 0.00001
NM_006393.3(NEBL):c.2547C>T (p.Gly849=) rs180850975 0.00001
NM_006393.3(NEBL):c.276C>T (p.Thr92=) rs1256058724 0.00001
NM_006393.3(NEBL):c.2820C>T (p.His940=) rs532565487 0.00001
NM_006393.3(NEBL):c.2913C>T (p.Asp971=) rs575423101 0.00001
NM_006393.3(NEBL):c.986G>T (p.Gly329Val) rs776185255 0.00001
NM_006393.3(NEBL):c.-20A>G rs766280453
NM_006393.3(NEBL):c.-9A>G rs772236141
NM_006393.3(NEBL):c.1269A>G (p.Lys423=) rs138932199
NM_006393.3(NEBL):c.1311A>G (p.Ala437=) rs901799820
NM_006393.3(NEBL):c.1339-11G>A
NM_006393.3(NEBL):c.1732C>T (p.Pro578Ser)
NM_006393.3(NEBL):c.1775C>A (p.Ala592Glu) rs146275785
NM_006393.3(NEBL):c.1775C>T (p.Ala592Val) rs146275785
NM_006393.3(NEBL):c.1962+14T>G rs1292029849
NM_006393.3(NEBL):c.2055+7C>A rs368793318
NM_006393.3(NEBL):c.228T>C (p.His76=) rs1057523090
NM_006393.3(NEBL):c.2475C>T (p.His825=) rs727503334
NM_006393.3(NEBL):c.2484C>T (p.Ile828=) rs1315850585
NM_006393.3(NEBL):c.255T>C (p.Ser85=) rs727504471
NM_006393.3(NEBL):c.259-21_259-15delinsCCTGG rs1554799332
NM_006393.3(NEBL):c.2748G>T (p.Pro916=) rs778128527
NM_006393.3(NEBL):c.342A>G (p.Ala114=)
NM_006393.3(NEBL):c.369+18T>C rs771142727
NM_006393.3(NEBL):c.480+10C>A rs377230358
NM_006393.3(NEBL):c.480+15_480+16del rs1064794541
NM_006393.3(NEBL):c.614A>G (p.Asn205Ser) rs794729077

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