DACT3[gene] and "single gene"[properties] - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2309682	NM_145056.3(DACT3):c.1861G>T (p.Gly621Cys)	DACT3 (G621C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079983	NM_145056.3(DACT3):c.1807G>C (p.Val603Leu)	DACT3 (V603L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242524	NM_145056.3(DACT3):c.1807G>T (p.Val603Leu)	DACT3 (V603L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079982	NM_145056.3(DACT3):c.1567G>A (p.Glu523Lys)	DACT3 (E298K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307466	NM_145056.3(DACT3):c.1478G>C (p.Arg493Pro)	DACT3 (R268P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512098	NM_145056.3(DACT3):c.1439C>T (p.Ala480Val)	DACT3 (A480V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333556	NM_145056.3(DACT3):c.1375C>T (p.Arg459Cys)	DACT3 (R234C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590755	NM_145056.3(DACT3):c.1306G>A (p.Ala436Thr)	DACT3 (A211T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614671	NM_145056.3(DACT3):c.1259A>G (p.Lys420Arg)	DACT3 (K195R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329458	NM_145056.3(DACT3):c.1258A>G (p.Lys420Glu)	DACT3 (K195E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606029	NM_145056.3(DACT3):c.1241G>C (p.Gly414Ala)	DACT3 (G189A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621455	NM_145056.3(DACT3):c.1234C>T (p.Arg412Cys)	DACT3 (R187C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079978	NM_145056.3(DACT3):c.1172C>T (p.Ser391Leu)	DACT3 (S166L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274520	NM_145056.3(DACT3):c.1111C>T (p.Pro371Ser)	DACT3 (P146S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346581	NM_145056.3(DACT3):c.1096G>C (p.Ala366Pro)	DACT3 (A366P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079977	NM_145056.3(DACT3):c.1088C>T (p.Ala363Val)	DACT3 (A138V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410697	NM_145056.3(DACT3):c.1072C>G (p.Gln358Glu)	DACT3 (Q133E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242245	NM_145056.3(DACT3):c.1018C>T (p.Pro340Ser)	DACT3 (P340S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079976	NM_145056.3(DACT3):c.1012G>C (p.Ala338Pro)	DACT3 (A338P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479898	NM_145056.3(DACT3):c.873C>A (p.Asp291Glu)	DACT3 (D66E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079990	NM_145056.3(DACT3):c.871G>A (p.Asp291Asn)	DACT3 (D66N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079989	NM_145056.3(DACT3):c.869C>T (p.Pro290Leu)	DACT3 (P65L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396636	NM_145056.3(DACT3):c.863G>T (p.Arg288Leu)	DACT3 (R288L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349387	NM_145056.3(DACT3):c.856C>T (p.Arg286Cys)	DACT3 (R286C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596833	NM_145056.3(DACT3):c.836C>T (p.Pro279Leu)	DACT3 (P279L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079987	NM_145056.3(DACT3):c.815C>T (p.Pro272Leu)	DACT3 (P272L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463996	NM_145056.3(DACT3):c.812G>C (p.Ser271Thr)	DACT3 (S271T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213171	NM_145056.3(DACT3):c.802C>A (p.Pro268Thr)	DACT3 (P268T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079986	NM_145056.3(DACT3):c.800A>C (p.Gln267Pro)	DACT3 (Q267P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256449	NM_145056.3(DACT3):c.788G>C (p.Arg263Pro)	DACT3 (R263P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590745	NM_145056.3(DACT3):c.785G>T (p.Arg262Leu)	DACT3 (R37L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 619120	NM_145056.3(DACT3):c.751G>T (p.Gly251Cys)	DACT3 (G251C +1 more)	Single nucleotide variant (missense variant)	Intellectual disability +1 more	GUncertain significance
Select item 2367802	NM_145056.3(DACT3):c.736G>C (p.Gly246Arg)	DACT3 (G246R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396168	NM_145056.3(DACT3):c.716C>T (p.Ser239Leu)	DACT3 (S14L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079985	NM_145056.3(DACT3):c.695G>A (p.Cys232Tyr)	DACT3 (C232Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079984	NM_145056.3(DACT3):c.637G>A (p.Gly213Arg)	DACT3 (G213R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2327341	NM_145056.3(DACT3):c.611C>T (p.Ser204Phe)	DACT3 (S204F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2605205	NM_145056.3(DACT3):c.541G>A (p.Ala181Thr)	DACT3 (A181T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2314902	NM_145056.3(DACT3):c.535G>C (p.Ala179Pro)	DACT3 (A179P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2340764	NM_145056.3(DACT3):c.344C>T (p.Ser115Leu)	DACT3 (S115L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2247780	NM_145056.3(DACT3):c.338G>C (p.Arg113Pro)	DACT3 (R113P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 41