"Ambry Genetics"[submitter] AND "ADAMTS6"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2295148	NM_197941.4(ADAMTS6):c.3182G>A (p.Arg1061Gln)	ADAMTS6 (R1061Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2603592	NM_197941.4(ADAMTS6):c.3148G>C (p.Gly1050Arg)	ADAMTS6 (G1050R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2373552	NM_197941.4(ADAMTS6):c.3032G>A (p.Arg1011His)	ADAMTS6 (R1011H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2470545	NM_197941.4(ADAMTS6):c.3031C>T (p.Arg1011Cys)	ADAMTS6 (R1011C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2347248	NM_197941.4(ADAMTS6):c.3025C>G (p.Arg1009Gly)	ADAMTS6 (R1009G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2553812	NM_197941.4(ADAMTS6):c.2977A>G (p.Lys993Glu)	ADAMTS6 (K993E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2397131	NM_197941.4(ADAMTS6):c.2791G>A (p.Gly931Arg)	ADAMTS6 (G931R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2372553	NM_197941.4(ADAMTS6):c.2727G>C (p.Leu909Phe)	ADAMTS6 (L909F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2210588	NM_197941.4(ADAMTS6):c.2302A>G (p.Ile768Val)	ADAMTS6 (I768V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2623681	NM_197941.4(ADAMTS6):c.2105G>A (p.Arg702Lys)	ADAMTS6 (R702K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2205487	NM_197941.4(ADAMTS6):c.2091G>T (p.Leu697Phe)	ADAMTS6 (L697F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2535510	NM_197941.4(ADAMTS6):c.1940T>G (p.Val647Gly)	ADAMTS6 (V647G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2365543	NM_197941.4(ADAMTS6):c.1861G>C (p.Glu621Gln)	ADAMTS6 (E621Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2562028	NM_197941.4(ADAMTS6):c.1850G>A (p.Arg617Gln)	ADAMTS6 (R617Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2304364	NM_197941.4(ADAMTS6):c.1847C>T (p.Ser616Phe)	ADAMTS6 (S616F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2458903	NM_197941.4(ADAMTS6):c.1775G>C (p.Gly592Ala)	ADAMTS6 (G592A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2286273	NM_197941.4(ADAMTS6):c.1745T>G (p.Leu582Arg)	ADAMTS6 (L582R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2354811	NM_197941.4(ADAMTS6):c.1619G>A (p.Gly540Glu)	ADAMTS6 (G540E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2554652	NM_197941.4(ADAMTS6):c.1349A>G (p.Asp450Gly)	ADAMTS6 (D450G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2297123	NM_197941.4(ADAMTS6):c.1348G>T (p.Asp450Tyr)	ADAMTS6 (D450Y)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2316907	NM_197941.4(ADAMTS6):c.1319A>G (p.Asn440Ser)	ADAMTS6 (N440S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2337116	NM_197941.4(ADAMTS6):c.1274A>G (p.His425Arg)	ADAMTS6 (H425R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2265523	NM_197941.4(ADAMTS6):c.1163G>A (p.Ser388Asn)	ADAMTS6 (S388N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2298871	NM_197941.4(ADAMTS6):c.731G>A (p.Arg244Lys)	ADAMTS6 (R244K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2283915	NM_197941.4(ADAMTS6):c.608A>T (p.Asp203Val)	ADAMTS6 (D203V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2493286	NM_197941.4(ADAMTS6):c.437T>C (p.Val146Ala)	ADAMTS6 (V146A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2530230	NM_197941.4(ADAMTS6):c.244G>A (p.Val82Ile)	ADAMTS6 (V82I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2492411	NM_197941.4(ADAMTS6):c.227T>G (p.Ile76Ser)	ADAMTS6 (I76S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2471995	NM_197941.4(ADAMTS6):c.36G>C (p.Leu12Phe)	ADAMTS6 (L12F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 29