"Ambry Genetics"[submitter] AND "CCAR1"[gene] - ClinVar

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Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2595802	NM_018237.4(CCAR1):c.121A>G (p.Ile41Val)	CCAR1 (I41V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532875	NM_018237.4(CCAR1):c.457G>A (p.Val153Met)	CCAR1 (V153M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263740	NM_018237.4(CCAR1):c.668C>G (p.Pro223Arg)	CCAR1 (P223R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138183	NM_018237.4(CCAR1):c.753G>C (p.Gln251His)	CCAR1 (Q236H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601421	NM_018237.4(CCAR1):c.865C>T (p.Pro289Ser)	CCAR1 (P274S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263738	NM_018237.4(CCAR1):c.899G>A (p.Arg300Gln)	CCAR1 (R300Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298281	NM_018237.4(CCAR1):c.1034G>A (p.Arg345Gln)	CCAR1 (R345Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2570488	NM_018237.4(CCAR1):c.1057C>T (p.Arg353Trp)	CCAR1 (R338W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263737	NM_018237.4(CCAR1):c.1070G>T (p.Arg357Leu)	CCAR1 (R342L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516524	NM_018237.4(CCAR1):c.1121C>T (p.Pro374Leu)	CCAR1 (P359L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138177	NM_018237.4(CCAR1):c.1124G>T (p.Ser375Ile)	CCAR1 (S360I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379366	NM_018237.4(CCAR1):c.1133T>C (p.Met378Thr)	CCAR1 (M378T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236576	NM_018237.4(CCAR1):c.1151G>A (p.Arg384His)	CCAR1 (R384H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311499	NM_018237.4(CCAR1):c.1337G>A (p.Ser446Asn)	CCAR1 (S431N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613033	NM_018237.4(CCAR1):c.1361G>C (p.Ser454Thr)	CCAR1 (S454T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210938	NM_018237.4(CCAR1):c.1424G>A (p.Arg475Gln)	CCAR1 (R475Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138178	NM_018237.4(CCAR1):c.1609A>T (p.Ser537Cys)	CCAR1 (S537C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551086	NM_018237.4(CCAR1):c.1610G>A (p.Ser537Asn)	CCAR1 (S522N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255936	NM_018237.4(CCAR1):c.1818G>T (p.Lys606Asn)	CCAR1 (K591N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474899	NM_018237.4(CCAR1):c.2038A>G (p.Lys680Glu)	CCAR1 (K665E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2465117	NM_018237.4(CCAR1):c.2076T>A (p.Asp692Glu)	CCAR1 (D677E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2407194	NM_018237.4(CCAR1):c.2180C>T (p.Pro727Leu)	CCAR1 (P727L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2303185	NM_018237.4(CCAR1):c.2431A>G (p.Arg811Gly)	CCAR1 (R811G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544529	NM_018237.4(CCAR1):c.2480C>T (p.Pro827Leu)	CCAR1 (P812L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279907	NM_018237.4(CCAR1):c.2597A>C (p.Asn866Thr)	CCAR1 (N866T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138179	NM_018237.4(CCAR1):c.2621A>G (p.Glu874Gly)	CCAR1 (E874G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463142	NM_018237.4(CCAR1):c.2630A>C (p.Glu877Ala)	CCAR1 (E862A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397588	NM_018237.4(CCAR1):c.2632G>T (p.Ala878Ser)	CCAR1 (A863S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138180	NM_018237.4(CCAR1):c.2696T>C (p.Ile899Thr)	CCAR1 (I899T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138181	NM_018237.4(CCAR1):c.2762T>A (p.Ile921Asn)	CCAR1 (I921N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3138182	NM_018237.4(CCAR1):c.2818C>T (p.Leu940Phe)	CCAR1 (L925F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337079	NM_018237.4(CCAR1):c.2888A>G (p.Lys963Arg)	CCAR1 (K963R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263739	NM_018237.4(CCAR1):c.2906T>C (p.Val969Ala)	CCAR1 (V969A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210291	NM_018237.4(CCAR1):c.2954A>C (p.Asp985Ala)	CCAR1 (D970A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494721	NM_018237.4(CCAR1):c.3103G>A (p.Gly1035Arg)	CCAR1 (G1035R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263736	NM_018237.4(CCAR1):c.3133G>A (p.Glu1045Lys)	CCAR1 (E1045K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534821	NM_018237.4(CCAR1):c.3151G>T (p.Val1051Leu)	CCAR1 (V1051L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613213	NM_018237.4(CCAR1):c.3398A>G (p.Asn1133Ser)	CCAR1 (N1118S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251785	NM_018237.4(CCAR1):c.3421C>A (p.Gln1141Lys)	CCAR1 (Q1141K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 39