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

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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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