Related gene-specific medical variations for Gene (Select 8756) - ClinVar

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Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3266150	NM_003817.4(ADAM7):c.1712G>C (p.Gly571Ala)	ADAM7, ADAM7-AS1 +1 more (G571A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3266142	NM_003817.4(ADAM7):c.1918A>C (p.Asn640His)	ADAM7, ADAM7-AS1 +1 more (N640H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3266141	NM_003817.4(ADAM7):c.1096C>T (p.Pro366Ser)	ADAM7, ADAM7-AS1 (P366S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3266130	NM_003817.4(ADAM7):c.1367C>T (p.Ala456Val)	ADAM7, ADAM7-AS1 +1 more (A456V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3266124	NM_003817.4(ADAM7):c.1741C>A (p.Pro581Thr)	ADAM7, ADAM7-AS1 +1 more (P581T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3266113	NM_003817.4(ADAM7):c.1354C>G (p.Gln452Glu)	ADAM7, ADAM7-AS1 +1 more (Q452E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3266103	NM_003817.4(ADAM7):c.310A>G (p.Met104Val)	ADAM7, ADAM7-AS1 (M104V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145976	NM_003817.4(ADAM7):c.919G>A (p.Gly307Arg)	ADAM7, ADAM7-AS1 (G307R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145967	NM_003817.4(ADAM7):c.865G>A (p.Val289Ile)	ADAM7, ADAM7-AS1 (V289I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145965	NM_003817.4(ADAM7):c.808C>T (p.Arg270Cys)	ADAM7, ADAM7-AS1 (R270C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145957	NM_003817.4(ADAM7):c.791T>C (p.Ile264Thr)	ADAM7, ADAM7-AS1 (I264T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145953	NM_003817.4(ADAM7):c.584T>C (p.Ile195Thr)	ADAM7, ADAM7-AS1 (I195T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145949	NM_003817.4(ADAM7):c.32T>C (p.Leu11Ser)	ADAM7, ADAM7-AS1 (L11S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145947	NM_003817.4(ADAM7):c.301C>A (p.Pro101Thr)	ADAM7, ADAM7-AS1 (P101T)	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 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 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 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 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 3145882	NM_003817.4(ADAM7):c.1236G>T (p.Glu412Asp)	ADAM7, ADAM7-AS1 (E412D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145878	NM_003817.4(ADAM7):c.1178T>C (p.Ile393Thr)	ADAM7, ADAM7-AS1 (I393T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145870	NM_003817.4(ADAM7):c.1154A>G (p.Tyr385Cys)	ADAM7, ADAM7-AS1 (Y385C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658485	NM_003817.4(ADAM7):c.1845G>C (p.Val615=)	ADAM7, ADAM7-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 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 2587913	NM_003817.4(ADAM7):c.804A>T (p.Leu268Phe)	ADAM7, ADAM7-AS1 (L268F)	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 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 2535096	NM_003817.4(ADAM7):c.982A>C (p.Ile328Leu)	ADAM7, ADAM7-AS1 (I328L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495811	NM_003817.4(ADAM7):c.1108T>C (p.Phe370Leu)	ADAM7, ADAM7-AS1 (F370L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493524	NM_003817.4(ADAM7):c.1029G>A (p.Met343Ile)	ADAM7, ADAM7-AS1 (M343I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491660	NM_003817.4(ADAM7):c.396C>A (p.Phe132Leu)	ADAM7, ADAM7-AS1 (F132L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389666	NM_003817.4(ADAM7):c.886C>T (p.Leu296Phe)	ADAM7, ADAM7-AS1 (L296F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381713	NM_003817.4(ADAM7):c.1171C>T (p.Leu391Phe)	ADAM7, ADAM7-AS1 (L391F)	Single nucleotide variant (missense variant)	not specified	GLikely benign
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 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 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 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 2360918	NM_003817.4(ADAM7):c.571A>G (p.Lys191Glu)	ADAM7, ADAM7-AS1 (K191E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357594	NM_003817.4(ADAM7):c.236A>T (p.Glu79Val)	ADAM7, ADAM7-AS1 (E79V)	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 2327193	NM_003817.4(ADAM7):c.501T>A (p.Asn167Lys)	ADAM7, ADAM7-AS1 (N167K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313447	NM_003817.4(ADAM7):c.1249G>A (p.Asp417Asn)	ADAM7, ADAM7-AS1 (D417N)	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 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 2287259	NM_003817.4(ADAM7):c.279A>C (p.Lys93Asn)	ADAM7, ADAM7-AS1 (K93N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282215	NM_003817.4(ADAM7):c.986T>C (p.Ile329Thr)	ADAM7, ADAM7-AS1 (I329T)	Single nucleotide variant (missense variant)	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 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 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
Select item 2250791	NM_003817.4(ADAM7):c.1166G>A (p.Cys389Tyr)	ADAM7, ADAM7-AS1 (C389Y)	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 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 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 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 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 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 873299	NM_003817.4(ADAM7):c.633+3318dup	ADAM7, ADAM7-AS1	Duplication (intron variant)	not specified	GBenign

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Links from Gene

Items: 58