"Ambry Genetics"[submitter] AND "LOC129995014"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2304858	NM_016221.4(DCTN4):c.95A>G (p.Tyr32Cys)	DCTN4, LOC129995014 (Y32C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080655	NM_016221.4(DCTN4):c.65C>T (p.Ala22Val)	DCTN4, LOC129995014 (A22V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080654	NM_016221.4(DCTN4):c.61C>G (p.Arg21Gly)	DCTN4, LOC129995014 (R21G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496509	NM_016221.4(DCTN4):c.26G>T (p.Arg9Leu)	DCTN4, LOC129995014 (R9L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080653	NM_016221.4(DCTN4):c.17A>T (p.Gln6Leu)	DCTN4, LOC129995014 (Q6L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548411	NM_016221.4(DCTN4):c.4G>T (p.Ala2Ser)	DCTN4, LOC129995014 (A2S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar