"Ambry Genetics"[submitter] AND "ADAM7-AS2"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2236869	NM_003817.4(ADAM7):c.1325G>A (p.Cys442Tyr)	ADAM7, ADAM7-AS1 +1 more (C442Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242464	NM_003817.4(ADAM7):c.1337A>G (p.Glu446Gly)	ADAM7, ADAM7-AS1 +1 more (E446G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222597	NM_003817.4(ADAM7):c.1364A>G (p.Lys455Arg)	ADAM7, ADAM7-AS1 +1 more (K455R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2290857	NM_003817.4(ADAM7):c.1388C>A (p.Ala463Glu)	ADAM7, ADAM7-AS1 +1 more (A463E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3145898	NM_003817.4(ADAM7):c.1457G>A (p.Arg486Lys)	ADAM7, ADAM7-AS1 +1 more (R486K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2205499	NM_003817.4(ADAM7):c.1475G>A (p.Cys492Tyr)	ADAM7, ADAM7-AS1 +1 more (C492Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2279822	NM_003817.4(ADAM7):c.1500C>A (p.Phe500Leu)	ADAM7, ADAM7-AS1 +1 more (F500L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3145910	NM_003817.4(ADAM7):c.1632C>G (p.Asn544Lys)	ADAM7, ADAM7-AS1 +1 more (N544K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372674	NM_003817.4(ADAM7):c.1667G>A (p.Cys556Tyr)	ADAM7, ADAM7-AS1 +1 more (C556Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537290	NM_003817.4(ADAM7):c.1769A>G (p.Lys590Arg)	ADAM7, ADAM7-AS1 +1 more (K590R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555796	NM_003817.4(ADAM7):c.1774A>C (p.Ile592Leu)	ADAM7, ADAM7-AS1 +1 more (I592L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259416	NM_003817.4(ADAM7):c.1786C>A (p.His596Asn)	ADAM7, ADAM7-AS1 +1 more (H596N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210025	NM_003817.4(ADAM7):c.1810G>C (p.Val604Leu)	ADAM7, ADAM7-AS1 +1 more (V604L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204092	NM_003817.4(ADAM7):c.1837G>C (p.Gly613Arg)	ADAM7, ADAM7-AS1 +1 more (G613R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308249	NM_003817.4(ADAM7):c.1981G>A (p.Glu661Lys)	ADAM7, ADAM7-AS1 +1 more (E661K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145923	NM_003817.4(ADAM7):c.2026C>T (p.Leu676Phe)	ADAM7, ADAM7-AS1 +1 more (L676F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145924	NM_003817.4(ADAM7):c.2041G>A (p.Val681Ile)	ADAM7, ADAM7-AS1 +1 more (V681I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2591596	NM_003817.4(ADAM7):c.2050G>A (p.Gly684Arg)	ADAM7, ADAM7-AS1 +1 more (G684R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348207	NM_003817.4(ADAM7):c.2072G>A (p.Arg691His)	ADAM7, ADAM7-AS1 +1 more (R691H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614746	NM_003817.4(ADAM7):c.2141A>T (p.Lys714Ile)	ADAM7, ADAM7-AS1 +1 more (K714I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145925	NM_003817.4(ADAM7):c.2163G>C (p.Gln721His)	ADAM7, ADAM7-AS1 +1 more (Q721H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368739	NM_003817.4(ADAM7):c.2183T>A (p.Ile728Asn)	ADAM7, ADAM7-AS1 +1 more (I728N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368740	NM_003817.4(ADAM7):c.2184C>G (p.Ile728Met)	ADAM7, ADAM7-AS1 +1 more (I728M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366056	NM_003817.4(ADAM7):c.2213C>T (p.Pro738Leu)	ADAM7, ADAM7-AS1 +1 more (P738L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256053	NM_003817.4(ADAM7):c.2239G>A (p.Ala747Thr)	ADAM7, ADAM7-AS1 +1 more (A747T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25