"Ambry Genetics"[submitter] AND "ARID5B"[gene] - ClinVar

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Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2273179	NM_032199.3(ARID5B):c.35C>A (p.Pro12Gln)	ARID5B (P12Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252863	NM_032199.3(ARID5B):c.140C>A (p.Thr47Lys)	ARID5B (T47K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315159	NM_032199.3(ARID5B):c.337G>C (p.Val113Leu)	ARID5B, LOC130003875 (V113L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129508	NM_032199.3(ARID5B):c.342T>G (p.His114Gln)	ARID5B, LOC130003875 (H114Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271402	NM_032199.3(ARID5B):c.434A>G (p.Lys145Arg)	ARID5B (K145R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492027	NM_032199.3(ARID5B):c.460G>A (p.Gly154Arg)	ARID5B (G154R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597762	NM_032199.3(ARID5B):c.481C>A (p.Leu161Ile)	ARID5B (L161I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129510	NM_032199.3(ARID5B):c.487G>C (p.Glu163Gln)	ARID5B (E163Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250995	NM_032199.3(ARID5B):c.658C>T (p.Pro220Ser)	ARID5B (P220S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129511	NM_032199.3(ARID5B):c.680A>C (p.Asp227Ala)	ARID5B (D227A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314870	NM_032199.3(ARID5B):c.784A>G (p.Arg262Gly)	ARID5B, LOC126860943 (R262G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462014	NM_032199.3(ARID5B):c.821A>G (p.Asn274Ser)	ARID5B, LOC126860943 (N274S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524873	NM_032199.3(ARID5B):c.996G>C (p.Met332Ile)	ARID5B (M332I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372142	NM_032199.3(ARID5B):c.1005G>C (p.Arg335Ser)	ARID5B (R335S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511228	NM_032199.3(ARID5B):c.1330A>G (p.Ile444Val)	ARID5B (I201V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397320	NM_032199.3(ARID5B):c.1343T>C (p.Ile448Thr)	ARID5B (I205T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129499	NM_032199.3(ARID5B):c.1352G>A (p.Ser451Asn)	ARID5B (S208N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129500	NM_032199.3(ARID5B):c.1563C>G (p.Asp521Glu)	ARID5B (D521E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557814	NM_032199.3(ARID5B):c.1652A>T (p.Lys551Ile)	ARID5B (K308I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487322	NM_032199.3(ARID5B):c.1654G>C (p.Asp552His)	ARID5B (D309H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314859	NM_032199.3(ARID5B):c.1665G>C (p.Leu555Phe)	ARID5B (L555F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312872	NM_032199.3(ARID5B):c.1706C>T (p.Ala569Val)	ARID5B (A326V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129501	NM_032199.3(ARID5B):c.1748C>T (p.Thr583Ile)	ARID5B (T583I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258438	NM_032199.3(ARID5B):c.1764T>A (p.Ser588Arg)	ARID5B (S588R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391794	NM_032199.3(ARID5B):c.1811C>T (p.Pro604Leu)	ARID5B (P361L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290973	NM_032199.3(ARID5B):c.1856T>C (p.Met619Thr)	ARID5B (M376T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522225	NM_032199.3(ARID5B):c.1886A>C (p.Lys629Thr)	ARID5B (K629T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375155	NM_032199.3(ARID5B):c.1909G>T (p.Asp637Tyr)	ARID5B (D394Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320659	NM_032199.3(ARID5B):c.1933A>T (p.Thr645Ser)	ARID5B (T645S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243311	NM_032199.3(ARID5B):c.1991G>A (p.Gly664Glu)	ARID5B (G664E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321975	NM_032199.3(ARID5B):c.2107A>G (p.Ser703Gly)	ARID5B (S703G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314889	NM_032199.3(ARID5B):c.2143C>A (p.Pro715Thr)	ARID5B (P715T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345111	NM_032199.3(ARID5B):c.2143C>G (p.Pro715Ala)	ARID5B (P715A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398832	NM_032199.3(ARID5B):c.2178T>A (p.Asp726Glu)	ARID5B (D483E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359329	NM_032199.3(ARID5B):c.2231T>C (p.Met744Thr)	ARID5B (M501T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360327	NM_032199.3(ARID5B):c.2234C>T (p.Ala745Val)	ARID5B (A745V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525686	NM_032199.3(ARID5B):c.2263G>A (p.Val755Ile)	ARID5B (V755I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129503	NM_032199.3(ARID5B):c.2354G>A (p.Arg785His)	ARID5B (R542H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303019	NM_032199.3(ARID5B):c.2362T>A (p.Phe788Ile)	ARID5B (F545I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555308	NM_032199.3(ARID5B):c.2461C>G (p.His821Asp)	ARID5B (H578D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222953	NM_032199.3(ARID5B):c.2471T>C (p.Met824Thr)	ARID5B (M581T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129504	NM_032199.3(ARID5B):c.2617C>T (p.His873Tyr)	ARID5B (H873Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129505	NM_032199.3(ARID5B):c.2635C>T (p.Leu879Phe)	ARID5B (L879F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473753	NM_032199.3(ARID5B):c.3020G>C (p.Gly1007Ala)	ARID5B (G764A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129506	NM_032199.3(ARID5B):c.3089C>T (p.Ala1030Val)	ARID5B (A787V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478117	NM_032199.3(ARID5B):c.3170C>T (p.Ala1057Val)	ARID5B (A1057V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129507	NM_032199.3(ARID5B):c.3203G>T (p.Gly1068Val)	ARID5B (G1068V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314880	NM_032199.3(ARID5B):c.3217C>T (p.Leu1073Phe)	ARID5B (L1073F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484297	NM_032199.3(ARID5B):c.3327G>C (p.Gln1109His)	ARID5B (Q866H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528225	NM_032199.3(ARID5B):c.3378G>A (p.Met1126Ile)	ARID5B (M883I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129509	NM_032199.3(ARID5B):c.3508C>A (p.Pro1170Thr)	ARID5B (P927T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 51