Variants in gene DCTN1 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_004082.5(DCTN1):c.3146G>A (p.Arg1049Gln)	rs72659383	0.00166
NM_004082.5(DCTN1):c.837G>A (p.Ala279=)	rs72466489	0.00020
NM_004082.5(DCTN1):c.1997C>T (p.Thr666Met)	rs143914684	0.00010
NM_004082.5(DCTN1):c.2353C>T (p.Arg785Trp)	rs121909344	0.00010
NM_004082.5(DCTN1):c.2278A>G (p.Met760Val)	rs754780894	0.00007
NM_004082.5(DCTN1):c.2002C>T (p.His668Tyr)	rs764443534	0.00006
NM_004082.5(DCTN1):c.3010C>G (p.Leu1004Val)	rs758387062	0.00006
NM_004082.5(DCTN1):c.60G>A (p.Ala20=)	rs150204862	0.00005
NM_004082.5(DCTN1):c.442C>T (p.Arg148Trp)	rs148810193	0.00003
NM_004082.5(DCTN1):c.3699+16G>A	rs747490958	0.00002

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