ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 94
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HGVS dbSNP
NM_213569.2(NEBL):c.204A>T (p.Thr68=) rs563150056
NM_213569.2(NEBL):c.250-214A>G
NM_213569.2(NEBL):c.250-215T>G
NM_213569.2(NEBL):c.357+64639A>G rs368268112
NM_213569.2(NEBL):c.357+64657T>C
NM_213569.2(NEBL):c.357+64722G>C
NM_213569.2(NEBL):c.357+71569T>C
NM_213569.2(NEBL):c.357+71749G>C rs41277374
NM_213569.2(NEBL):c.357+72010A>C
NM_213569.2(NEBL):c.357+73457T>C
NM_213569.2(NEBL):c.357+73473C>G rs147622517
NM_213569.2(NEBL):c.357+73500T>A
NM_213569.2(NEBL):c.357+73506T>C
NM_213569.2(NEBL):c.357+73573G>A rs189440246
NM_213569.2(NEBL):c.357+73580G>A rs200249470
NM_213569.2(NEBL):c.357T>C (p.Asn119=) rs115708584
NM_213569.2(NEBL):c.358-10018G>A
NM_213569.2(NEBL):c.358-10261A>G rs371630900
NM_213569.2(NEBL):c.358-10276A>C rs200756166
NM_213569.2(NEBL):c.358-10337A>G
NM_213569.2(NEBL):c.358-10352C>T rs551329782
NM_213569.2(NEBL):c.358-10360G>C
NM_213569.2(NEBL):c.358-1038T>C rs144815863
NM_213569.2(NEBL):c.358-13538G>A rs151035799
NM_213569.2(NEBL):c.358-13542G>A rs778658096
NM_213569.2(NEBL):c.358-13549A>G
NM_213569.2(NEBL):c.358-1410G>A
NM_213569.2(NEBL):c.358-15591C>A rs146275785
NM_213569.2(NEBL):c.358-17968T>C
NM_213569.2(NEBL):c.358-18152A>G
NM_213569.2(NEBL):c.358-18458C>T
NM_213569.2(NEBL):c.358-18647G>A
NM_213569.2(NEBL):c.358-22383A>G
NM_213569.2(NEBL):c.358-2686C>T
NM_213569.2(NEBL):c.358-2694T>C
NM_213569.2(NEBL):c.358-2720G>T rs780056247
NM_213569.2(NEBL):c.358-27835C>G rs202112717
NM_213569.2(NEBL):c.358-39529C>T
NM_213569.2(NEBL):c.358-39601_358-39600inv
NM_213569.2(NEBL):c.358-39619G>A rs150518045
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.358-45366A>G
NM_213569.2(NEBL):c.358-45376T>C rs141285752
NM_213569.2(NEBL):c.358-45656A>G
NM_213569.2(NEBL):c.358-4656T>C rs193163659
NM_213569.2(NEBL):c.358-4669C>T
NM_213569.2(NEBL):c.358-46779G>A rs375771045
NM_213569.2(NEBL):c.358-46794T>G
NM_213569.2(NEBL):c.358-46851G>A
NM_213569.2(NEBL):c.358-47191T>A
NM_213569.2(NEBL):c.358-4728C>T rs114875104
NM_213569.2(NEBL):c.358-55726C>G rs143644290
NM_213569.2(NEBL):c.358-55804G>A rs137973321
NM_213569.2(NEBL):c.358-56629G>T
NM_213569.2(NEBL):c.358-56821G>C rs75301590
NM_213569.2(NEBL):c.358-57058A>C
NM_213569.2(NEBL):c.358-6476G>A
NM_213569.2(NEBL):c.358-6484G>A
NM_213569.2(NEBL):c.358-6485C>T rs146218038
NM_213569.2(NEBL):c.358-6561C>A rs11012351
NM_213569.2(NEBL):c.358-67844C>A rs377230358
NM_213569.2(NEBL):c.358-67884T>C
NM_213569.2(NEBL):c.358-67896T>C rs780880217
NM_213569.2(NEBL):c.358-67899C>T
NM_213569.2(NEBL):c.358-67929A>C
NM_213569.2(NEBL):c.358-67951A>T rs139809958
NM_213569.2(NEBL):c.358-68192A>G
NM_213569.2(NEBL):c.358-9C>T rs750957531
NM_213569.2(NEBL):c.406C>T (p.Pro136Ser)
NM_213569.2(NEBL):c.408C>T (p.Pro136=) rs766216481
NM_213569.2(NEBL):c.417C>T (p.Asp139=)
NM_213569.2(NEBL):c.529+10C>A
NM_213569.2(NEBL):c.529+10C>T rs747607700
NM_213569.2(NEBL):c.529+2899C>T rs180850975
NM_213569.2(NEBL):c.529+3050del
NM_213569.2(NEBL):c.529+4117G>A rs140803920
NM_213569.2(NEBL):c.529+4152C>T rs143584663
NM_213569.2(NEBL):c.529+4171A>G rs202127185
NM_213569.2(NEBL):c.529+4222A>T rs146673676
NM_213569.2(NEBL):c.529+4255A>G rs878854903
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.530-7C>T
NM_213569.2(NEBL):c.543C>T (p.Pro181=) rs199887353
NM_213569.2(NEBL):c.615A>T (p.Ser205=) rs1060504994
NM_213569.2(NEBL):c.637-10C>G rs373167913
NM_213569.2(NEBL):c.657C>T (p.Tyr219=) rs202184399
NM_213569.2(NEBL):c.699C>T (p.Asp233=)
NM_213569.2(NEBL):c.711C>T (p.Ile237=)
NM_213569.2(NEBL):c.732C>T (p.Asp244=) rs144946187

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