"Ambry Genetics"[submitter] AND "DCTN4"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2325059	NM_016221.4(DCTN4):c.1304T>C (p.Ile435Thr)	DCTN4 (I435T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620218	NM_016221.4(DCTN4):c.1292C>T (p.Pro431Leu)	DCTN4 (P374L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224744	NM_016221.4(DCTN4):c.1270G>C (p.Asp424His)	DCTN4 (D424H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470817	NM_016221.4(DCTN4):c.1243G>A (p.Val415Met)	DCTN4 (V358M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557927	NM_016221.4(DCTN4):c.1238G>A (p.Gly413Asp)	DCTN4 (G413D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370390	NM_016221.4(DCTN4):c.1213A>G (p.Lys405Glu)	DCTN4 (K348E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226167	NM_016221.4(DCTN4):c.1162G>A (p.Asp388Asn)	DCTN4 (D331N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080652	NM_016221.4(DCTN4):c.1096G>A (p.Val366Ile)	DCTN4 (V309I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2551169	NM_016221.4(DCTN4):c.1061G>A (p.Ser354Asn)	DCTN4 (S354N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219621	NM_016221.4(DCTN4):c.832C>T (p.Arg278Cys)	DCTN4 (R278C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271160	NM_016221.4(DCTN4):c.818G>A (p.Arg273Gln)	DCTN4 (R273Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483636	NM_016221.4(DCTN4):c.817C>T (p.Arg273Trp)	DCTN4 (R280W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080657	NM_016221.4(DCTN4):c.707C>T (p.Pro236Leu)	DCTN4 (P179L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080656	NM_016221.4(DCTN4):c.706C>T (p.Pro236Ser)	DCTN4 (P179S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271159	NM_016221.4(DCTN4):c.604G>A (p.Gly202Arg)	DCTN4 (G209R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596951	NM_016221.4(DCTN4):c.485G>A (p.Arg162Gln)	DCTN4 (R105Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344543	NM_016221.4(DCTN4):c.427C>T (p.Arg143Trp)	DCTN4 (R86W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219990	NM_016221.4(DCTN4):c.394G>A (p.Gly132Ser)	DCTN4 (G75S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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

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Items: 24