List of variants reported as likely benign for Perry syndrome

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_004082.5(DCTN1):c.2258C>T (p.Thr753Met)	rs143763184	0.00179
NM_004082.5(DCTN1):c.3610-14C>T	rs757854575	0.00038
NM_004082.5(DCTN1):c.3490A>G (p.Thr1164Ala)	rs72466493	0.00024
NM_004082.5(DCTN1):c.*49G>A	rs368049781	0.00013
NM_004082.5(DCTN1):c.2002C>T (p.His668Tyr)	rs764443534	0.00006
NM_004082.5(DCTN1):c.60G>A (p.Ala20=)	rs150204862	0.00005
NM_004082.5(DCTN1):c.673C>T (p.Arg225Trp)	rs371723224	0.00004
NM_004082.5(DCTN1):c.2633A>G (p.Tyr878Cys)	rs778201974	0.00003
NM_004082.5(DCTN1):c.1059C>T (p.Gly353=)	rs771325809	0.00001
NM_004082.5(DCTN1):c.3712C>G (p.Gln1238Glu)	rs778307537	0.00001

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