List of variants in gene NEB reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 38

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.18862G>A (p.Val6288Ile)	rs201886728	0.00066
NM_001164508.2(NEB):c.20956G>C (p.Asp6986His)	rs150874422	0.00055
NM_001164508.2(NEB):c.20654C>T (p.Ala6885Val)	rs202209668	0.00054
NM_001164508.2(NEB):c.9139C>A (p.His3047Asn)	rs147168910	0.00022
NM_001164508.2(NEB):c.7309C>T (p.Arg2437Trp)	rs375164626	0.00016
NM_001164508.2(NEB):c.10583G>A (p.Arg3528His)	rs199584268	0.00015
NM_001164508.2(NEB):c.1544A>G (p.Gln515Arg)	rs368150737	0.00014
NM_001164508.2(NEB):c.10802A>G (p.His3601Arg)	rs371568550	0.00013
NM_001164508.2(NEB):c.1550A>G (p.Asn517Ser)	rs199710125	0.00013
NM_001164508.2(NEB):c.19966C>T (p.Arg6656Cys)	rs527250558	0.00011
NM_001164508.2(NEB):c.6481C>T (p.Arg2161Cys)	rs201758329	0.00011
NM_001164508.2(NEB):c.10181T>C (p.Ile3394Thr)	rs376182104	0.00010
NM_001164508.2(NEB):c.17462G>A (p.Arg5821His)	rs773239926	0.00010
NM_001164508.2(NEB):c.18859C>T (p.Arg6287Cys)	rs374606967	0.00010
NM_001164508.2(NEB):c.4904C>T (p.Thr1635Ile)	rs199662534	0.00010
NM_001164508.2(NEB):c.5495T>C (p.Ile1832Thr)	rs751494785	0.00010
NM_001164508.2(NEB):c.11077C>T (p.Arg3693Cys)	rs539139958	0.00009
NM_001164508.2(NEB):c.20245C>A (p.Gln6749Lys)	rs772854423	0.00007
NM_001164508.2(NEB):c.11717G>A (p.Arg3906His)	rs556930902	0.00006
NM_001164508.2(NEB):c.5939T>C (p.Leu1980Ser)	rs375412223	0.00006
NM_001164508.2(NEB):c.7861G>A (p.Asp2621Asn)	rs781745506	0.00005
NM_001164508.2(NEB):c.20132G>A (p.Arg6711Gln)	rs781250495	0.00004
NM_001164508.2(NEB):c.3571G>A (p.Val1191Ile)	rs767493706	0.00004
NM_001164508.2(NEB):c.19724G>A (p.Arg6575His)	rs185999504	0.00003
NM_001164508.2(NEB):c.19861C>T (p.His6621Tyr)	rs1559832482	0.00002
NM_001164508.2(NEB):c.4666C>T (p.Pro1556Ser)	rs756692621	0.00002
NM_001164508.2(NEB):c.9853C>T (p.Arg3285Cys)	rs370572955	0.00002
NM_001164508.2(NEB):c.9875T>C (p.Ile3292Thr)	rs186634689	0.00002
NM_001164508.2(NEB):c.1613A>G (p.His538Arg)	rs925195870	0.00001
NM_001164508.2(NEB):c.17197C>T (p.Arg5733Cys)	rs1000108046	0.00001
NM_001164508.2(NEB):c.20033G>A (p.Arg6678His)	rs1487589344	0.00001
NM_001164508.2(NEB):c.6262G>A (p.Val2088Ile)	rs747729019	0.00001
NM_001164508.2(NEB):c.8381A>T (p.Tyr2794Phe)	rs750548574	0.00001
NM_001164508.2(NEB):c.18694-6_18694-2del	rs1377029367
NM_001164508.2(NEB):c.20442_20447dup (p.Ser6815_Arg6816dup)	rs760783104
NM_001164508.2(NEB):c.3127_3129dup (p.Asn1043dup)	rs1288870299
NM_001164508.2(NEB):c.5224C>T (p.Leu1742=)	rs886054947
NM_001164508.2(NEB):c.5698_5703del (p.Tyr1900_Asn1901del)	rs775531807

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