"Ambry Genetics"[submitter] AND "ARVCF"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3147939	NM_000754.4(COMT):c.685T>C (p.Phe229Leu)	ARVCF, COMT (F229L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352410	NM_000754.4(COMT):c.700C>T (p.Arg234Cys)	ARVCF, COMT (R234C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289835	NM_000754.4(COMT):c.718G>C (p.Glu240Gln)	ARVCF, COMT (E190Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336011	NM_000754.4(COMT):c.756G>C (p.Glu252Asp)	ARVCF, COMT (E202D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1335474	NM_001670.3(ARVCF):c.2872G>A (p.Val958Ile)	ARVCF (V958I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2476815	NM_001670.3(ARVCF):c.2848G>A (p.Val950Ile)	ARVCF (V881I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130004	NM_001670.3(ARVCF):c.2846C>T (p.Ala949Val)	ARVCF (A880V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316844	NM_001670.3(ARVCF):c.2812G>A (p.Gly938Arg)	ARVCF (G869R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524512	NM_001670.3(ARVCF):c.2803C>T (p.Pro935Ser)	ARVCF (P866S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308054	NM_001670.3(ARVCF):c.2797A>G (p.Lys933Glu)	ARVCF (K864E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316882	NM_001670.3(ARVCF):c.2768A>C (p.Lys923Thr)	ARVCF (K923T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130003	NM_001670.3(ARVCF):c.2764G>A (p.Glu922Lys)	ARVCF (E853K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130001	NM_001670.3(ARVCF):c.2735G>A (p.Arg912Gln)	ARVCF (R912Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488825	NM_001670.3(ARVCF):c.2705C>A (p.Ser902Tyr)	ARVCF (S902Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259417	NM_001670.3(ARVCF):c.2693C>A (p.Pro898Gln)	ARVCF (P898Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598592	NM_001670.3(ARVCF):c.2674C>T (p.Pro892Ser)	ARVCF (P823S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593635	NM_001670.3(ARVCF):c.2661C>G (p.Ser887Arg)	ARVCF (S887R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130000	NM_001670.3(ARVCF):c.2657G>T (p.Gly886Val)	ARVCF (G817V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328547	NM_001670.3(ARVCF):c.2644G>A (p.Gly882Ser)	ARVCF (G882S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391419	NM_001670.3(ARVCF):c.2615C>T (p.Thr872Met)	ARVCF (T872M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129999	NM_001670.3(ARVCF):c.2599G>T (p.Gly867Cys)	ARVCF (G867C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317527	NM_001670.3(ARVCF):c.2555C>G (p.Ala852Gly)	ARVCF (A783G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406278	NM_001670.3(ARVCF):c.2525A>C (p.Asp842Ala)	ARVCF (D773A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129998	NM_001670.3(ARVCF):c.2513C>G (p.Thr838Ser)	ARVCF (T769S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481679	NM_001670.3(ARVCF):c.2513C>T (p.Thr838Ile)	ARVCF (T769I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273269	NM_001670.3(ARVCF):c.2476C>G (p.Leu826Val)	ARVCF (L826V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316879	NM_001670.3(ARVCF):c.2435C>A (p.Ser812Tyr)	ARVCF (S812Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316825	NM_001670.3(ARVCF):c.2398G>T (p.Ala800Ser)	ARVCF (A731S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316872	NM_001670.3(ARVCF):c.2339T>C (p.Leu780Pro)	ARVCF (L780P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618233	NM_001670.3(ARVCF):c.2297G>A (p.Arg766Gln)	ARVCF (R697Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129997	NM_001670.3(ARVCF):c.2135C>T (p.Pro712Leu)	ARVCF (P643L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129996	NM_001670.3(ARVCF):c.2081A>G (p.Asn694Ser)	ARVCF (N625S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129995	NM_001670.3(ARVCF):c.2072G>A (p.Ser691Asn)	ARVCF (S622N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225439	NM_001670.3(ARVCF):c.2068C>T (p.Leu690Phe)	ARVCF (L690F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129994	NM_001670.3(ARVCF):c.2050G>A (p.Ala684Thr)	ARVCF (A615T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341843	NM_001670.3(ARVCF):c.1993C>T (p.Arg665Cys)	ARVCF (R596C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552646	NM_001670.3(ARVCF):c.1987G>T (p.Val663Leu)	ARVCF (V663L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286430	NM_001670.3(ARVCF):c.1913G>A (p.Arg638Gln)	ARVCF (R638Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591248	NM_001670.3(ARVCF):c.1893G>C (p.Lys631Asn)	ARVCF (K631N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316878	NM_001670.3(ARVCF):c.1856G>A (p.Gly619Asp)	ARVCF (G556D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517624	NM_001670.3(ARVCF):c.1832G>A (p.Arg611Gln)	ARVCF (R548Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129993	NM_001670.3(ARVCF):c.1825C>T (p.Arg609Trp)	ARVCF (R546W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129992	NM_001670.3(ARVCF):c.1823G>A (p.Arg608His)	ARVCF (R608H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607146	NM_001670.3(ARVCF):c.1796C>T (p.Pro599Leu)	ARVCF (P536L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337777	NM_001670.3(ARVCF):c.1705G>A (p.Glu569Lys)	ARVCF (E569K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227397	NM_001670.3(ARVCF):c.1684G>A (p.Asp562Asn)	ARVCF (D562N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600644	NM_001670.3(ARVCF):c.1622G>A (p.Arg541Gln)	ARVCF (R541Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510672	NM_001670.3(ARVCF):c.1618C>T (p.Leu540Phe)	ARVCF (L477F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598172	NM_001670.3(ARVCF):c.1613G>A (p.Arg538Gln)	ARVCF (R538Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392960	NM_001670.3(ARVCF):c.1610G>A (p.Arg537Gln)	ARVCF (R474Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129990	NM_001670.3(ARVCF):c.1583A>G (p.Asn528Ser)	ARVCF (N528S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129989	NM_001670.3(ARVCF):c.1565C>T (p.Thr522Met)	ARVCF (T522M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409584	NM_001670.3(ARVCF):c.1531C>T (p.Arg511Trp)	ARVCF (R511W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533604	NM_001670.3(ARVCF):c.1309G>A (p.Ala437Thr)	ARVCF (A437T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129988	NM_001670.3(ARVCF):c.1279C>A (p.Leu427Ile)	ARVCF (L364I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129987	NM_001670.3(ARVCF):c.1265G>T (p.Gly422Val)	ARVCF (G422V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617149	NM_001670.3(ARVCF):c.1249C>T (p.Arg417Trp)	ARVCF (R417W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316852	NM_001670.3(ARVCF):c.1180C>T (p.Arg394Trp)	ARVCF (R331W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306733	NM_001670.3(ARVCF):c.1167C>G (p.Asn389Lys)	ARVCF (N326K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129986	NM_001670.3(ARVCF):c.1120G>T (p.Val374Leu)	ARVCF (V311L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311648	NM_001670.3(ARVCF):c.1120G>A (p.Val374Met)	ARVCF (V374M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129985	NM_001670.3(ARVCF):c.1111G>A (p.Val371Met)	ARVCF (V308M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129984	NM_001670.3(ARVCF):c.1063T>C (p.Trp355Arg)	ARVCF (W292R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316829	NM_001670.3(ARVCF):c.1060C>A (p.Arg354Ser)	ARVCF (R354S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471176	NM_001670.3(ARVCF):c.1049G>A (p.Arg350His)	ARVCF (R350H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381223	NM_001670.3(ARVCF):c.1011C>G (p.Asp337Glu)	ARVCF (D274E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241598	NM_001670.3(ARVCF):c.985G>A (p.Glu329Lys)	ARVCF (E329K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523775	NM_001670.3(ARVCF):c.982C>G (p.Pro328Ala)	ARVCF (P328A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221243	NM_001670.3(ARVCF):c.968C>T (p.Ala323Val)	ARVCF (A323V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372316	NM_001670.3(ARVCF):c.917A>T (p.Asp306Val)	ARVCF (D243V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394826	NM_001670.3(ARVCF):c.851C>T (p.Thr284Met)	ARVCF (T284M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206145	NM_001670.3(ARVCF):c.797G>A (p.Arg266His)	ARVCF (R203H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362743	NM_001670.3(ARVCF):c.794C>T (p.Thr265Met)	ARVCF (T202M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254489	NM_001670.3(ARVCF):c.779G>C (p.Gly260Ala)	ARVCF (G260A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130013	NM_001670.3(ARVCF):c.758G>A (p.Arg253His)	ARVCF (R190H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130012	NM_001670.3(ARVCF):c.748C>G (p.Leu250Val)	ARVCF (L187V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217693	NM_001670.3(ARVCF):c.742C>T (p.Arg248Cys)	ARVCF (R185C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130011	NM_001670.3(ARVCF):c.715G>T (p.Gly239Cys)	ARVCF (G176C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130010	NM_001670.3(ARVCF):c.709C>A (p.Pro237Thr)	ARVCF (P174T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592010	NM_001670.3(ARVCF):c.646G>T (p.Gly216Cys)	ARVCF (G216C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458746	NM_001670.3(ARVCF):c.631C>T (p.Arg211Trp)	ARVCF (R211W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594671	NM_001670.3(ARVCF):c.586C>T (p.Arg196Trp)	ARVCF (R133W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371489	NM_001670.3(ARVCF):c.580G>A (p.Glu194Lys)	ARVCF (E131K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130008	NM_001670.3(ARVCF):c.556G>A (p.Gly186Arg)	ARVCF (G123R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341095	NM_001670.3(ARVCF):c.539G>A (p.Arg180Gln)	ARVCF (R117Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130007	NM_001670.3(ARVCF):c.533T>A (p.Leu178His)	ARVCF (L115H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130006	NM_001670.3(ARVCF):c.532C>T (p.Leu178Phe)	ARVCF (L178F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343179	NM_001670.3(ARVCF):c.494G>A (p.Arg165Gln)	ARVCF (R165Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514998	NM_001670.3(ARVCF):c.461C>G (p.Pro154Arg)	ARVCF (P91R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333537	NM_001670.3(ARVCF):c.439C>T (p.Pro147Ser)	ARVCF (P147S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323130	NM_001670.3(ARVCF):c.415G>T (p.Val139Leu)	ARVCF (V76L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623436	NM_001670.3(ARVCF):c.395C>T (p.Thr132Ile)	ARVCF (T132I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524034	NM_001670.3(ARVCF):c.370G>A (p.Val124Ile)	ARVCF (V124I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316836	NM_001670.3(ARVCF):c.337G>A (p.Glu113Lys)	ARVCF (E50K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310204	NM_001670.3(ARVCF):c.311C>T (p.Thr104Ile)	ARVCF (T41I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602874	NM_001670.3(ARVCF):c.278C>A (p.Thr93Asn)	ARVCF (T93N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282542	NM_001670.3(ARVCF):c.137A>G (p.Gln46Arg)	ARVCF (Q46R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129983	NM_001670.3(ARVCF):c.101G>A (p.Arg34Gln)	ARVCF (R34Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371764	NM_001670.3(ARVCF):c.70G>A (p.Glu24Lys)	ARVCF (E24K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316858	NM_001670.3(ARVCF):c.64C>T (p.Arg22Cys)	ARVCF (R22C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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