ClinVar Miner

List of variants in gene NEBL reported as likely benign by Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_213569.2(NEBL):c.204A>T (p.Thr68=) rs563150056
NM_213569.2(NEBL):c.357+64522G>A rs727503338
NM_213569.2(NEBL):c.357+64639A>G rs368268112
NM_213569.2(NEBL):c.357+64681A>G rs397517203
NM_213569.2(NEBL):c.357+64729T>G rs397517204
NM_213569.2(NEBL):c.357+71712C>A rs41277376
NM_213569.2(NEBL):c.357+71749G>C rs41277374
NM_213569.2(NEBL):c.357+71809C>T rs727503337
NM_213569.2(NEBL):c.357+71824T>C rs727504471
NM_213569.2(NEBL):c.358-10261A>G rs371630900
NM_213569.2(NEBL):c.358-10276A>C rs200756166
NM_213569.2(NEBL):c.358-15591C>A rs146275785
NM_213569.2(NEBL):c.358-15638T>C rs1528182
NM_213569.2(NEBL):c.358-22559G>A rs373699154
NM_213569.2(NEBL):c.358-27835C>G rs202112717
NM_213569.2(NEBL):c.358-27865A>G rs727504866
NM_213569.2(NEBL):c.358-27868A>G rs138932199
NM_213569.2(NEBL):c.358-27916C>T rs200231082
NM_213569.2(NEBL):c.358-39590G>A rs375728589
NM_213569.2(NEBL):c.358-39597C>G rs376842299
NM_213569.2(NEBL):c.358-39619G>A rs150518045
NM_213569.2(NEBL):c.358-56893T>C rs141153708
NM_213569.2(NEBL):c.358-6477C>A rs368793318
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.358-9C>T rs750957531
NM_213569.2(NEBL):c.456G>A (p.Val152=) rs578252294
NM_213569.2(NEBL):c.486C>T (p.His162=) rs727503334
NM_213569.2(NEBL):c.493A>G (p.Ile165Val) rs143930021
NM_213569.2(NEBL):c.529+2899C>T rs180850975
NM_213569.2(NEBL):c.529+4152C>T rs143584663
NM_213569.2(NEBL):c.529+4246G>T rs778128527
NM_213569.2(NEBL):c.529+4274C>T rs760162209
NM_213569.2(NEBL):c.543C>T (p.Pro181=) rs199887353
NM_213569.2(NEBL):c.588C>T (p.His196=) rs532565487
NM_213569.2(NEBL):c.681C>T (p.Asp227=) rs575423101
NM_213569.2(NEBL):c.69+15G>T rs377648518

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