"Ambry Genetics"[submitter] AND "ADAM22"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2372577	NM_001324418.2(ADAM22):c.71G>C (p.Arg24Pro)	ADAM22, LOC129998760 (R24P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2401856	NM_001324418.2(ADAM22):c.77G>T (p.Gly26Val)	ADAM22, LOC129998760 (G26V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2370262	NM_001324418.2(ADAM22):c.77G>A (p.Gly26Asp)	ADAM22, LOC129998760 (G26D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2274915	NM_001324418.2(ADAM22):c.359T>C (p.Ile120Thr)	ADAM22 (I137T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2340254	NM_001324418.2(ADAM22):c.367G>A (p.Gly123Arg)	ADAM22 (G122R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2325136	NM_001324418.2(ADAM22):c.433C>T (p.Pro145Ser)	ADAM22 (P144S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2363099	NM_001324418.2(ADAM22):c.665G>T (p.Arg222Met)	ADAM22 (R222M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2468678	NM_001324418.2(ADAM22):c.734T>C (p.Ile245Thr)	ADAM22 (I245T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2224473	NM_001324418.2(ADAM22):c.775G>A (p.Val259Ile)	ADAM22 (V258I +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2328403	NM_001324418.2(ADAM22):c.794A>C (p.Tyr265Ser)	ADAM22 (Y282S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2344456	NM_001324418.2(ADAM22):c.992C>T (p.Ser331Leu)	ADAM22 (S323L +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334480	NM_001324418.2(ADAM22):c.1132A>C (p.Ile378Leu)	ADAM22 (I378L +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2331585	NM_001324418.2(ADAM22):c.1141A>G (p.Ile381Val)	ADAM22 (I381V +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2386143	NM_001324418.2(ADAM22):c.1573C>A (p.Pro525Thr)	ADAM22 (P524T +3 more)	Single nucleotide variant (missense variant)	ADAM22-related condition +1 more	GConflicting classifications of pathogenicity
Select item 2276336	NM_001324418.2(ADAM22):c.1700A>G (p.Lys567Arg)	ADAM22 (K584R +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2473773	NM_001324418.2(ADAM22):c.1790A>C (p.Asp597Ala)	ADAM22 (D589A +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2557358	NM_001324418.2(ADAM22):c.1848A>C (p.Glu616Asp)	ADAM22 (E633D +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2411525	NM_001324418.2(ADAM22):c.1889G>A (p.Gly630Glu)	ADAM22 (G630E +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488926	NM_001324418.2(ADAM22):c.1893A>C (p.Arg631Ser)	ADAM22 (R623S +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2407776	NM_001324418.2(ADAM22):c.2026T>C (p.Phe676Leu)	ADAM22 (F693L +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2483743	NM_001324418.2(ADAM22):c.2165A>C (p.Lys722Thr)	ADAM22 (K722T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2515932	NM_001324418.2(ADAM22):c.2190T>A (p.Asn730Lys)	ADAM22 (N729K +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2547202	NM_001324418.2(ADAM22):c.2191+6T>C	ADAM22	Single nucleotide variant (intron variant)	Inborn genetic diseases	GUncertain significance
Select item 2606694	NM_001324418.2(ADAM22):c.2249C>T (p.Ala750Val)	ADAM22 (A749V +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334913	NM_001324418.2(ADAM22):c.2303A>G (p.Gln768Arg)	ADAM22 (Q768R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2488621	NM_001324418.2(ADAM22):c.2647C>T (p.Arg883Trp)	ADAM22 (R817W +8 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2295536	NM_001324418.2(ADAM22):c.2738G>A (p.Gly913Glu)	ADAM22 (G902E +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 27