List of variants in gene NEB reported as benign for not provided

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: 75

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.9124T>C (p.Cys3042Arg)	rs6710212	0.97529
NM_001164508.2(NEB):c.3081A>T (p.Lys1027Asn)	rs6735208	0.69255
NM_001164508.2(NEB):c.771T>C (p.Ala257=)	rs4611637	0.68008
NM_001164508.2(NEB):c.18305G>C (p.Arg6102Thr)	rs2288210	0.66332
NM_001164508.2(NEB):c.4471G>A (p.Val1491Met)	rs7426114	0.66326
NM_001164508.2(NEB):c.9363T>C (p.Pro3121=)	rs6709886	0.62301
NM_001164508.2(NEB):c.7839G>C (p.Lys2613Asn)	rs13013209	0.34676
NM_001164508.2(NEB):c.8734T>C (p.Ser2912Pro)	rs6713162	0.31314
NM_001164508.2(NEB):c.5370G>A (p.Glu1790=)	rs10170273	0.30371
NM_001164508.2(NEB):c.6807+6T>G	rs10930723	0.29833
NM_001164508.2(NEB):c.16705-18C>T	rs61254943	0.26527
NM_001164508.2(NEB):c.10809G>C (p.Trp3603Cys)	rs10172023	0.26237
NM_001164508.2(NEB):c.18294T>C (p.Tyr6098=)	rs2288211	0.24726
NM_001164508.2(NEB):c.11077-19T>C	rs4303716	0.21438
NM_001164508.2(NEB):c.4435G>A (p.Val1479Ile)	rs34577613	0.20341
NM_001164508.2(NEB):c.3901= (p.Tyr1301=)	rs6711382	0.18897
NM_001164508.2(NEB):c.16911A>G (p.Pro5637=)	rs33988153	0.17490
NM_001164508.2(NEB):c.2944-9G>A	rs13427102	0.10205
NM_001164508.2(NEB):c.6184-14T>A	rs10173335	0.09664
NM_001164508.2(NEB):c.8466C>T (p.His2822=)	rs61730771	0.02236
NM_001164508.2(NEB):c.16021T>C (p.Leu5341=)	rs796103760	0.02016
NM_001164508.2(NEB):c.8318G>A (p.Arg2773Gln)	rs35974308	0.01764
NM_001164508.2(NEB):c.18113A>G (p.Asn6038Ser)	rs16830236	0.01192
NM_001164508.2(NEB):c.5567G>A (p.Arg1856Gln)	rs141930814	0.01071
NM_001164508.2(NEB):c.21044C>G (p.Ser7015Cys)	rs62167164	0.00935
NM_001164508.2(NEB):c.11769T>C (p.Ile3923=)	rs80320923	0.00914
NM_001164508.2(NEB):c.19311C>T (p.Ser6437=)	rs16830216	0.00914
NM_001164508.2(NEB):c.10338T>C (p.Asn3446=)	rs147569843	0.00870
NM_001164508.2(NEB):c.10344C>T (p.Asn3448=)	rs145052299	0.00870
NM_001164508.2(NEB):c.10347+6C>T	rs141088433	0.00870
NM_001164508.2(NEB):c.6159G>A (p.Lys2053=)	rs140186806	0.00856
NM_001164508.2(NEB):c.16669A>G (p.Ile5557Val)	rs113439353	0.00852
NM_001164508.2(NEB):c.20078C>T (p.Thr6693Ile)	rs35707762	0.00734
NM_001164508.2(NEB):c.2832C>T (p.Ser944=)	rs114076205	0.00714
NM_001164508.2(NEB):c.3191A>G (p.Tyr1064Cys)	rs187343008	0.00681
NM_001164508.2(NEB):c.6069G>A (p.Met2023Ile)	rs184262608	0.00672
NM_001164508.2(NEB):c.8189A>G (p.Asp2730Gly)	rs76767949	0.00646
NM_001164508.2(NEB):c.16670T>C (p.Ile5557Thr)	rs200703673	0.00584
NM_001164508.2(NEB):c.17304G>A (p.Leu5768=)	rs35273905	0.00526
NM_001164508.2(NEB):c.17049G>T (p.Ala5683=)	rs140688592	0.00517
NM_001164508.2(NEB):c.18693G>C (p.Ala6231=)	rs141338915	0.00448
NM_001164508.2(NEB):c.12147G>A (p.Lys4049=)	rs149639365	0.00441
NM_001164508.2(NEB):c.2640C>T (p.Arg880=)	rs114959904	0.00433
NM_001164508.2(NEB):c.1856A>G (p.Lys619Arg)	rs147305883	0.00426
NM_001164508.2(NEB):c.1981C>T (p.Leu661=)	rs146460133	0.00395
NM_001164508.2(NEB):c.17747A>G (p.Lys5916Arg)	rs73967567	0.00393
NM_001164508.2(NEB):c.6166A>G (p.Arg2056Gly)	rs115350357	0.00379
NM_001164508.2(NEB):c.1413C>T (p.Phe471=)	rs112958786	0.00363
NM_001164508.2(NEB):c.19056G>T (p.Thr6352=)	rs115631125	0.00354
NM_001164508.2(NEB):c.5102T>C (p.Val1701Ala)	rs117271684	0.00348
NM_001164508.2(NEB):c.3412A>G (p.Asn1138Asp)	rs117048449	0.00346
NM_001164508.2(NEB):c.16284+6A>G	rs573898757	0.00338
NM_001164508.2(NEB):c.3636C>T (p.Asp1212=)	rs144376972	0.00333
NM_001164508.2(NEB):c.1675-9T>G	rs75118047	0.00324
NM_001164508.2(NEB):c.5968G>A (p.Glu1990Lys)	rs146310692	0.00320
NM_001164508.2(NEB):c.18861C>T (p.Arg6287=)	rs146294986	0.00286
NM_001164508.2(NEB):c.10744G>A (p.Val3582Ile)	rs139798654	0.00257
NM_001164508.2(NEB):c.4980C>T (p.Pro1660=)	rs142074817	0.00242
NM_001164508.2(NEB):c.10452+9A>G	rs117270796	0.00190
NM_001164508.2(NEB):c.11004G>A (p.Thr3668=)	rs117018177	0.00190
NM_001164508.2(NEB):c.914A>G (p.Asp305Gly)	rs36105240	0.00148
NM_001164508.2(NEB):c.9072G>A (p.Ala3024=)	rs369897667	0.00125
NM_001164508.2(NEB):c.12C>T (p.Asp4=)	rs117178114	0.00119
NM_001164508.2(NEB):c.177G>A (p.Gln59=)	rs200990309	0.00112
NM_001164508.2(NEB):c.9052G>A (p.Asp3018Asn)	rs192098032	0.00081
NM_001164508.2(NEB):c.17887G>A (p.Val5963Ile)	rs138217960	0.00079
NM_001164508.2(NEB):c.8801G>A (p.Arg2934His)	rs200307392	0.00039
NM_001164508.2(NEB):c.19295A>G (p.Gln6432Arg)	rs189912759	0.00019
NM_001164508.2(NEB):c.11181T>A (p.Asp3727Glu)	rs551261559	0.00002
NM_001164508.2(NEB):c.20089G>A (p.Gly6697Arg)	rs201071685	0.00001
NM_001164508.2(NEB):c.11077-7_11077-5dup	rs749915004
NM_001164508.2(NEB):c.14563T>C (p.Leu4855=)	rs2288217
NM_001164508.2(NEB):c.153_167dup (p.52LAQPA[3])	rs757726895
NM_001164508.2(NEB):c.19285_19286delinsAA (p.Ala6429Asn)	rs796065338
NM_001164508.2(NEB):c.9467T>A (p.Ile3156Asn)	rs145770770

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