List of variants reported as benign for nemaline myopathy by Natera, Inc.

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

Total variants: 104

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HGVS	dbSNP	gnomAD frequency
NM_001164508.2(NEB):c.9124T>C (p.Cys3042Arg)	rs6710212	0.97679
NM_001164508.2(NEB):c.3901T>C (p.Tyr1301His)	rs6711382	0.80679
NM_001164508.2(NEB):c.3081A>T (p.Lys1027Asn)	rs6735208	0.69087
NM_001164508.2(NEB):c.771T>C (p.Ala257=)	rs4611637	0.67903
NM_001164508.2(NEB):c.4471G>A (p.Val1491Met)	rs7426114	0.66326
NM_001164508.2(NEB):c.18305G>C (p.Arg6102Thr)	rs2288210	0.66275
NM_001164508.2(NEB):c.24433G>C (p.Ala8145Pro)	rs7575451	0.64120
NM_001164508.2(NEB):c.9363T>C (p.Pro3121=)	rs6709886	0.62301
NM_001164508.2(NEB):c.21585A>G (p.Thr7195=)	rs4664475	0.55659
NM_001164508.2(NEB):c.25204A>G (p.Ile8402Val)	rs1061305	0.39905
NM_001164508.2(NEB):c.7839G>C (p.Lys2613Asn)	rs13013209	0.34960
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.10809G>C (p.Trp3603Cys)	rs10172023	0.26237
NM_001164508.2(NEB):c.18294T>C (p.Tyr6098=)	rs2288211	0.24726
NM_001164508.2(NEB):c.4435G>A (p.Val1479Ile)	rs34577613	0.20341
NM_001164508.2(NEB):c.16911A>G (p.Pro5637=)	rs33988153	0.17490
NM_001164508.2(NEB):c.13628A>C (p.Lys4543Thr)	rs200125713	0.16543
NM_001164508.2(NEB):c.11077-4G>T	rs878924060	0.11336
NM_001164508.2(NEB):c.2944-9G>A	rs13427102	0.09971
NM_001164508.2(NEB):c.10707G>A (p.Lys3569=)	rs6717213	0.08304
NM_001164508.2(NEB):c.16450G>A (p.Ala5484Thr)	rs536508687	0.08083
NM_001164508.2(NEB):c.13721A>G (p.His4574Arg)	rs876657542	0.07088
NM_001164508.2(NEB):c.5971C>T (p.His1991Tyr)	rs75807392	0.05468
NM_001164508.2(NEB):c.20598C>G (p.Gly6866=)	rs16830192	0.04050
NM_001164508.2(NEB):c.25395T>G (p.Ser8465=)	rs13031275	0.03886
NM_001164508.2(NEB):c.16762T>A (p.Ser5588Thr)	rs35227368	0.03610
NM_001164508.2(NEB):c.19102-6C>T	rs145127681	0.03008
NM_001164508.2(NEB):c.21382T>C (p.Leu7128=)	rs114218081	0.02605
NM_001164508.2(NEB):c.612+8T>C	rs113095802	0.02350
NM_001164508.2(NEB):c.8466C>T (p.His2822=)	rs61730771	0.02236
NM_001164508.2(NEB):c.7310G>A (p.Arg2437Gln)	rs61730780	0.02113
NM_001164508.2(NEB):c.8318G>A (p.Arg2773Gln)	rs35974308	0.01764
NM_001164508.2(NEB):c.21856G>A (p.Asp7286Asn)	rs35625617	0.01652
NM_001164508.2(NEB):c.571G>C (p.Glu191Gln)	rs35686968	0.01624
NM_001164508.2(NEB):c.11148G>C (p.Met3716Ile)	rs149025191	0.01369
NM_001164508.2(NEB):c.20766C>T (p.Asp6922=)	rs34555492	0.01319
NM_001164508.2(NEB):c.195G>A (p.Pro65=)	rs79524813	0.01277
NM_001164508.2(NEB):c.8592T>C (p.Asp2864=)	rs61730772	0.01264
NM_001164508.2(NEB):c.3775-6T>C	rs80232472	0.01222
NM_001164508.2(NEB):c.23511G>A (p.Thr7837=)	rs35808744	0.01201
NM_001164508.2(NEB):c.5772C>T (p.Tyr1924=)	rs77547727	0.01123
NM_001164508.2(NEB):c.6717T>G (p.Ile2239Met)	rs78733601	0.01102
NM_001164508.2(NEB):c.18113A>G (p.Asn6038Ser)	rs16830236	0.01099
NM_001164508.2(NEB):c.8646C>T (p.Asp2882=)	rs61730773	0.01069
NM_001164508.2(NEB):c.5763+4C>T	rs78916288	0.01001
NM_001164508.2(NEB):c.21519C>T (p.Ser7173=)	rs16830170	0.01000
NM_001164508.2(NEB):c.18555G>A (p.Lys6185=)	rs145252235	0.00972
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.10344C>T (p.Asn3448=)	rs145052299	0.00891
NM_001164508.2(NEB):c.10338T>C (p.Asn3446=)	rs147569843	0.00890
NM_001164508.2(NEB):c.6159G>A (p.Lys2053=)	rs140186806	0.00856
NM_001164508.2(NEB):c.8335A>G (p.Ile2779Val)	rs114853127	0.00849
NM_001164508.2(NEB):c.19311C>T (p.Ser6437=)	rs16830216	0.00846
NM_001164508.2(NEB):c.24208-7C>T	rs113048349	0.00793
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.5905T>C (p.Tyr1969His)	rs34532796	0.00550
NM_001164508.2(NEB):c.5802C>T (p.Gly1934=)	rs139963368	0.00529
NM_001164508.2(NEB):c.17049G>T (p.Ala5683=)	rs140688592	0.00517
NM_001164508.2(NEB):c.17304G>A (p.Leu5768=)	rs35273905	0.00493
NM_001164508.2(NEB):c.18693G>C (p.Ala6231=)	rs141338915	0.00484
NM_001164508.2(NEB):c.12147G>A (p.Lys4049=)	rs149639365	0.00441
NM_001164508.2(NEB):c.5102T>C (p.Val1701Ala)	rs117271684	0.00429
NM_001164508.2(NEB):c.1856A>G (p.Lys619Arg)	rs147305883	0.00426
NM_001164508.2(NEB):c.2640C>T (p.Arg880=)	rs114959904	0.00407
NM_001164508.2(NEB):c.17747A>G (p.Lys5916Arg)	rs73967567	0.00393
NM_001164508.2(NEB):c.19056G>T (p.Thr6352=)	rs115631125	0.00390
NM_001164508.2(NEB):c.6166A>G (p.Arg2056Gly)	rs115350357	0.00379
NM_001164508.2(NEB):c.1981C>T (p.Leu661=)	rs146460133	0.00360
NM_001164508.2(NEB):c.22904G>A (p.Gly7635Glu)	rs3732309	0.00351
NM_001164508.2(NEB):c.3412A>G (p.Asn1138Asp)	rs117048449	0.00346
NM_001164508.2(NEB):c.3826C>A (p.Pro1276Thr)	rs34234609	0.00327
NM_001164508.2(NEB):c.12667G>A (p.Ala4223Thr)	rs12998234	0.00244
NM_001164508.2(NEB):c.2318A>G (p.Tyr773Cys)	rs77151072	0.00241
NM_001164508.2(NEB):c.6615C>G (p.Arg2205=)	rs200018782	0.00226
NM_001164508.2(NEB):c.3348C>T (p.Asn1116=)	rs149162847	0.00217
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	0.00190
NM_001164508.2(NEB):c.21720C>T (p.Tyr7240=)	rs34718443	0.00171
NM_001164508.2(NEB):c.23599A>C (p.Lys7867Gln)	rs118191309	0.00171
NM_001164508.2(NEB):c.16449C>T (p.Ser5483=)	rs546992311	0.00148
NM_001164508.2(NEB):c.12770G>A (p.Arg4257His)	rs576918934	0.00147
NM_001164508.2(NEB):c.25035C>T (p.Asp8345=)	rs201825451	0.00131
NM_001164508.2(NEB):c.9072G>A (p.Ala3024=)	rs369897667	0.00125
NM_001164508.2(NEB):c.10463G>A (p.Arg3488His)	rs371605774	0.00088
NM_001164508.2(NEB):c.8499G>A (p.Lys2833=)	rs183998406	0.00083
NM_001164508.2(NEB):c.18783G>A (p.Gln6261=)	rs148095660	0.00081
NM_001164508.2(NEB):c.17887G>A (p.Val5963Ile)	rs138217960	0.00079
NM_001164508.2(NEB):c.20032C>T (p.Arg6678Cys)	rs200239095	0.00049
NM_001164508.2(NEB):c.18530G>A (p.Arg6177His)	rs147159176	0.00034
NM_001164508.2(NEB):c.23055G>A (p.Gly7685=)	rs563896790	0.00010
NM_001164508.2(NEB):c.863A>G (p.Lys288Arg)	rs202035863	0.00005
NM_001164508.2(NEB):c.10275G>A (p.Lys3425=)	rs1205545857
NM_001164508.2(NEB):c.14827-14CT[2]	rs536426422
NM_001164508.2(NEB):c.17635-3del	rs3214503
NM_001164508.2(NEB):c.17635-3dup	rs3214503
NM_001164508.2(NEB):c.18997-10T>C	rs4544436
NM_001164508.2(NEB):c.21418-6del	rs56026241
NM_001164508.2(NEB):c.21546C>T (p.Asn7182=)	rs149510427
NM_001164508.2(NEB):c.9346G>A (p.Glu3116Lys)	rs193042896

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