List of variants reported as benign for Nemaline myopathy 2 by Invitae

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Total variants: 26

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HGVS	dbSNP
NM_001271208.2(NEB):c.11148G>C (p.Met3716Ile)	rs149025191
NM_001271208.2(NEB):c.11729A>G (p.Asp3910Gly)	rs35740585
NM_001271208.2(NEB):c.16762T>A (p.Ser5588Thr)	rs35227368
NM_001271208.2(NEB):c.18555G>A (p.Lys6185=)	rs145252235
NM_001271208.2(NEB):c.18997-10T>C	rs4544436
NM_001271208.2(NEB):c.19102-6C>T	rs145127681
NM_001271208.2(NEB):c.19732-6C>T	rs11894996
NM_001271208.2(NEB):c.20192A>T (p.Asp6731Val)	rs2288200
NM_001271208.2(NEB):c.20598C>G (p.Gly6866=)	rs16830192
NM_001271208.2(NEB):c.20766C>T (p.Asp6922=)	rs34555492
NM_001271208.2(NEB):c.21487T>C (p.Leu7163=)	rs114218081
NM_001271208.2(NEB):c.21651C>T (p.Asn7217=)	rs149510427
NM_001271208.2(NEB):c.21961G>A (p.Asp7321Asn)	rs35625617
NM_001271208.2(NEB):c.22068A>G (p.Lys7356=)	rs61730765
NM_001271208.2(NEB):c.23486C>T (p.Ser7829Leu)	rs41270201
NM_001271208.2(NEB):c.24313-7C>T	rs113048349
NM_001271208.2(NEB):c.25500T>G (p.Ser8500=)	rs13031275
NM_001271208.2(NEB):c.3147+5G>A	rs74859201
NM_001271208.2(NEB):c.4407G>C (p.Glu1469Asp)	rs34800215
NM_001271208.2(NEB):c.5567G>A (p.Arg1856Gln)	rs141930814
NM_001271208.2(NEB):c.571G>C (p.Glu191Gln)	rs35686968
NM_001271208.2(NEB):c.612+8T>C	rs113095802
NM_001271208.2(NEB):c.7310G>A (p.Arg2437Gln)	rs61730780
NM_001271208.2(NEB):c.8318G>A (p.Arg2773Gln)	rs35974308
NM_001271208.2(NEB):c.8466C>T (p.His2822=)	rs61730771
NM_001271208.2(NEB):c.9467T>A (p.Ile3156Asn)	rs145770770

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