List of variants in gene NEBL reported as benign for Primary dilated cardiomyopathy

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

Total variants: 52

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HGVS	dbSNP	gnomAD frequency
NM_006393.3(NEBL):c.1008+5A>G	rs703089	0.98186
NM_006393.3(NEBL):c.480+3069G>A	rs3858198	0.55160
NM_006393.3(NEBL):c.1671+9T>C	rs10491056	0.42572
NM_006393.3(NEBL):c.2031G>A (p.Arg677=)	rs1006363	0.22278
NM_006393.3(NEBL):c.2997A>G (p.Thr999=)	rs2296614	0.08806
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.1008+4C>T	rs71534253	0.00540
NM_006393.3(NEBL):c.1117-6T>G	rs71578938	0.00538
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.1450-9T>G	rs45628140	0.00280
NM_006393.3(NEBL):c.2149-5G>A	rs71578956	0.00272
NM_006393.3(NEBL):c.154-11C>A	rs41277376	0.00252
NM_006393.3(NEBL):c.109T>C (p.Leu37=)	rs140734883	0.00213
NM_006393.3(NEBL):c.1869+8C>G	rs188529864	0.00188
NM_006393.3(NEBL):c.2685C>T (p.Asp895=)	rs140245727	0.00135
NM_006393.3(NEBL):c.2482A>G (p.Ile828Val)	rs143930021	0.00132
NM_006393.3(NEBL):c.624C>T (p.Pro208=)	rs111854914	0.00124
NM_006393.3(NEBL):c.1008+8C>G	rs376842299	0.00054
NM_006393.3(NEBL):c.27A>C (p.Ile9=)	rs536400111	0.00021
NM_006393.3(NEBL):c.1728T>C (p.Asp576=)	rs1528182	0.00019
NM_006393.3(NEBL):c.480+11G>A	rs769167750	0.00014
NM_006393.3(NEBL):c.393T>C (p.Asp131=)	rs759593690	0.00013
NM_006393.3(NEBL):c.120A>G (p.Glu40=)	rs397517203	0.00009
NM_006393.3(NEBL):c.582+9T>C	rs185873503	0.00009
NM_006393.3(NEBL):c.2612-11C>T	rs200934881	0.00008
NM_006393.3(NEBL):c.1272A>G (p.Gly424=)	rs727504866	0.00006
NM_006393.3(NEBL):c.1776+15C>G	rs373748632	0.00006
NM_006393.3(NEBL):c.2346+6G>A	rs201822024	0.00006
NM_006393.3(NEBL):c.993C>T (p.Ala331=)	rs375117092	0.00005
NM_006393.3(NEBL):c.1108C>A (p.Gln370Lys)	rs146198369	0.00004
NM_006393.3(NEBL):c.1116+17G>C	rs370094745	0.00004
NM_006393.3(NEBL):c.798+7T>A	rs771324301	0.00004
NM_006393.3(NEBL):c.153+15T>G	rs397517204	0.00003
NM_006393.3(NEBL):c.1776+10_1776+11insGCT	rs752802559	0.00003
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.1008+18C>T	rs75903914
NM_006393.3(NEBL):c.154-3dup	rs751577413
NM_006393.3(NEBL):c.1837C>A (p.Arg613=)	rs146471913
NM_006393.3(NEBL):c.2519-2del	rs754453916
NM_006393.3(NEBL):c.3021G>A (p.Ala1007=)
NM_006393.3(NEBL):c.82-8dup
NM_213569.2(NEBL):c.357+73449dup	rs57918610
NM_213569.2(NEBL):c.357+73457del	rs57918610

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