"Ambry Genetics"[submitter] AND "TNRC18"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3180675	NM_001080495.3(TNRC18):c.8903G>A (p.Cys2968Tyr)	TNRC18 (C2968Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540622	NM_001080495.3(TNRC18):c.8854G>A (p.Glu2952Lys)	TNRC18 (E2952K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383014	NM_001080495.3(TNRC18):c.8817G>C (p.Gln2939His)	TNRC18 (Q2939H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281477	NM_001080495.3(TNRC18):c.8682G>C (p.Gln2894His)	TNRC18 (Q2894H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460933	NM_001080495.3(TNRC18):c.8669G>A (p.Arg2890Gln)	TNRC18 (R2890Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372827	NM_001080495.3(TNRC18):c.8660C>T (p.Ala2887Val)	TNRC18 (A2887V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332582	NM_001080495.3(TNRC18):c.8654T>G (p.Leu2885Arg)	TNRC18 (L2885R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232014	NM_001080495.3(TNRC18):c.8616C>A (p.His2872Gln)	TNRC18 (H2872Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605282	NM_001080495.3(TNRC18):c.8587G>C (p.Glu2863Gln)	TNRC18 (E2863Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180672	NM_001080495.3(TNRC18):c.8519G>A (p.Arg2840His)	TNRC18 (R2840H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274987	NM_001080495.3(TNRC18):c.8452A>G (p.Met2818Val)	TNRC18 (M2818V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617318	NM_001080495.3(TNRC18):c.8441G>A (p.Arg2814His)	TNRC18 (R2814H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238677	NM_001080495.3(TNRC18):c.8419C>A (p.Leu2807Ile)	TNRC18 (L2807I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317374	NM_001080495.3(TNRC18):c.8338G>A (p.Ala2780Thr)	TNRC18 (A2780T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369974	NM_001080495.3(TNRC18):c.8263G>A (p.Val2755Ile)	TNRC18 (V2755I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180670	NM_001080495.3(TNRC18):c.8240G>A (p.Ser2747Asn)	TNRC18 (S2747N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286121	NM_001080495.3(TNRC18):c.8147C>T (p.Ser2716Phe)	TNRC18 (S2716F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180669	NM_001080495.3(TNRC18):c.8132G>A (p.Arg2711Gln)	TNRC18 (R2711Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379711	NM_001080495.3(TNRC18):c.8129C>T (p.Ala2710Val)	TNRC18 (A2710V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365651	NM_001080495.3(TNRC18):c.8072C>T (p.Ala2691Val)	TNRC18 (A2691V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479994	NM_001080495.3(TNRC18):c.8071G>A (p.Ala2691Thr)	TNRC18 (A2691T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219227	NM_001080495.3(TNRC18):c.8069C>T (p.Thr2690Met)	TNRC18 (T2690M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617456	NM_001080495.3(TNRC18):c.8047G>A (p.Asp2683Asn)	TNRC18 (D2683N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570210	NM_001080495.3(TNRC18):c.8033C>A (p.Ser2678Tyr)	TNRC18 (S2678Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463611	NM_001080495.3(TNRC18):c.8022C>G (p.Asp2674Glu)	TNRC18 (D2674E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180667	NM_001080495.3(TNRC18):c.7982C>T (p.Ser2661Phe)	TNRC18 (S2661F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180666	NM_001080495.3(TNRC18):c.7970C>T (p.Ser2657Phe)	TNRC18 (S2657F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556982	NM_001080495.3(TNRC18):c.7958C>T (p.Ser2653Phe)	TNRC18 (S2653F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458258	NM_001080495.3(TNRC18):c.7955C>T (p.Ser2652Phe)	TNRC18 (S2652F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306716	NM_001080495.3(TNRC18):c.7840T>G (p.Ser2614Ala)	TNRC18 (S2614A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613191	NM_001080495.3(TNRC18):c.7828G>A (p.Ala2610Thr)	TNRC18 (A2610T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613190	NM_001080495.3(TNRC18):c.7789A>G (p.Thr2597Ala)	TNRC18 (T2597A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3180664	NM_001080495.3(TNRC18):c.7732G>A (p.Gly2578Ser)	TNRC18 (G2578S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3180663	NM_001080495.3(TNRC18):c.7729A>G (p.Ser2577Gly)	TNRC18 (S2577G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357765	NM_001080495.3(TNRC18):c.7687A>G (p.Ser2563Gly)	TNRC18 (S2563G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236815	NM_001080495.3(TNRC18):c.7651C>G (p.Gln2551Glu)	TNRC18 (Q2551E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180662	NM_001080495.3(TNRC18):c.7631C>T (p.Pro2544Leu)	TNRC18 (P2544L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491363	NM_001080495.3(TNRC18):c.7620C>A (p.Asn2540Lys)	TNRC18 (N2540K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 794457	NM_001080495.3(TNRC18):c.7584G>T (p.Glu2528Asp)	TNRC18 (E2528D)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2365121	NM_001080495.3(TNRC18):c.7558G>A (p.Ala2520Thr)	TNRC18 (A2520T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180661	NM_001080495.3(TNRC18):c.7520C>T (p.Ala2507Val)	TNRC18 (A2507V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481400	NM_001080495.3(TNRC18):c.7516C>A (p.Pro2506Thr)	TNRC18 (P2506T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359777	NM_001080495.3(TNRC18):c.7513C>T (p.Pro2505Ser)	TNRC18 (P2505S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454613	NM_001080495.3(TNRC18):c.7486A>G (p.Lys2496Glu)	TNRC18 (K2496E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553795	NM_001080495.3(TNRC18):c.7450C>T (p.Arg2484Trp)	TNRC18 (R2484W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593633	NM_001080495.3(TNRC18):c.7436A>C (p.Glu2479Ala)	TNRC18 (E2479A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206692	NM_001080495.3(TNRC18):c.7375G>A (p.Glu2459Lys)	TNRC18 (E2459K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354110	NM_001080495.3(TNRC18):c.7361C>T (p.Pro2454Leu)	TNRC18 (P2454L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313827	NM_001080495.3(TNRC18):c.7348G>T (p.Gly2450Cys)	TNRC18 (G2450C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180659	NM_001080495.3(TNRC18):c.7300C>T (p.Arg2434Cys)	TNRC18 (R2434C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180658	NM_001080495.3(TNRC18):c.7291C>T (p.Pro2431Ser)	TNRC18 (P2431S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472556	NM_001080495.3(TNRC18):c.7180C>T (p.Pro2394Ser)	TNRC18 (P2394S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180657	NM_001080495.3(TNRC18):c.7172C>T (p.Pro2391Leu)	TNRC18 (P2391L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530106	NM_001080495.3(TNRC18):c.7169G>T (p.Arg2390Leu)	TNRC18 (R2390L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269707	NM_001080495.3(TNRC18):c.7163A>G (p.Lys2388Arg)	TNRC18 (K2388R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180656	NM_001080495.3(TNRC18):c.7141G>T (p.Asp2381Tyr)	TNRC18 (D2381Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517413	NM_001080495.3(TNRC18):c.7139T>C (p.Val2380Ala)	TNRC18 (V2380A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599715	NM_001080495.3(TNRC18):c.7119G>C (p.Lys2373Asn)	TNRC18 (K2373N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180655	NM_001080495.3(TNRC18):c.7111G>C (p.Gly2371Arg)	TNRC18 (G2371R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281476	NM_001080495.3(TNRC18):c.7103G>C (p.Ser2368Thr)	TNRC18 (S2368T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180654	NM_001080495.3(TNRC18):c.7099A>G (p.Ser2367Gly)	TNRC18 (S2367G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308475	NM_001080495.3(TNRC18):c.7082C>T (p.Pro2361Leu)	TNRC18 (P2361L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289813	NM_001080495.3(TNRC18):c.7077T>A (p.Ser2359Arg)	TNRC18 (S2359R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385341	NM_001080495.3(TNRC18):c.7072C>A (p.Pro2358Thr)	TNRC18 (P2358T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180653	NM_001080495.3(TNRC18):c.7057C>A (p.Pro2353Thr)	TNRC18 (P2353T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180652	NM_001080495.3(TNRC18):c.7054A>G (p.Asn2352Asp)	TNRC18 (N2352D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180651	NM_001080495.3(TNRC18):c.7023G>T (p.Lys2341Asn)	TNRC18 (K2341N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180650	NM_001080495.3(TNRC18):c.6988C>T (p.Arg2330Cys)	TNRC18 (R2330C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180649	NM_001080495.3(TNRC18):c.6965C>T (p.Ser2322Leu)	TNRC18 (S2322L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274764	NM_001080495.3(TNRC18):c.6956C>T (p.Thr2319Met)	TNRC18 (T2319M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 718825	NM_001080495.3(TNRC18):c.6818C>T (p.Pro2273Leu)	TNRC18 (P2273L)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2536039	NM_001080495.3(TNRC18):c.6755A>G (p.Asp2252Gly)	TNRC18 (D2252G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2301872	NM_001080495.3(TNRC18):c.6448C>G (p.Arg2150Gly)	TNRC18 (R2150G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616298	NM_001080495.3(TNRC18):c.6415G>A (p.Gly2139Arg)	TNRC18 (G2139R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180648	NM_001080495.3(TNRC18):c.6409C>T (p.Arg2137Cys)	TNRC18 (R2137C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180647	NM_001080495.3(TNRC18):c.6396C>G (p.Asp2132Glu)	TNRC18 (D2132E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180646	NM_001080495.3(TNRC18):c.6380C>T (p.Ser2127Leu)	TNRC18 (S2127L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180644	NM_001080495.3(TNRC18):c.6307G>A (p.Gly2103Ser)	TNRC18 (G2103S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527122	NM_001080495.3(TNRC18):c.6236C>T (p.Ala2079Val)	TNRC18 (A2079V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592698	NM_001080495.3(TNRC18):c.6235G>A (p.Ala2079Thr)	TNRC18 (A2079T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2301590	NM_001080495.3(TNRC18):c.6170G>A (p.Gly2057Glu)	TNRC18 (G2057E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474176	NM_001080495.3(TNRC18):c.6139C>A (p.Pro2047Thr)	TNRC18 (P2047T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406081	NM_001080495.3(TNRC18):c.6129C>G (p.Asp2043Glu)	TNRC18 (D2043E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303541	NM_001080495.3(TNRC18):c.6119G>C (p.Arg2040Pro)	TNRC18 (R2040P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260572	NM_001080495.3(TNRC18):c.6119G>T (p.Arg2040Leu)	TNRC18 (R2040L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180643	NM_001080495.3(TNRC18):c.6092C>T (p.Pro2031Leu)	TNRC18 (P2031L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457015	NM_001080495.3(TNRC18):c.6080C>T (p.Ala2027Val)	TNRC18 (A2027V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180642	NM_001080495.3(TNRC18):c.6074G>A (p.Arg2025His)	TNRC18 (R2025H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569064	NM_001080495.3(TNRC18):c.5987G>C (p.Arg1996Pro)	TNRC18 (R1996P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180641	NM_001080495.3(TNRC18):c.5923C>T (p.Arg1975Trp)	TNRC18 (R1975W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309583	NM_001080495.3(TNRC18):c.5897A>C (p.Glu1966Ala)	TNRC18 (E1966A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250976	NM_001080495.3(TNRC18):c.5882C>G (p.Ala1961Gly)	TNRC18 (A1961G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289425	NM_001080495.3(TNRC18):c.5864C>T (p.Pro1955Leu)	TNRC18 (P1955L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180640	NM_001080495.3(TNRC18):c.5860G>T (p.Asp1954Tyr)	TNRC18 (D1954Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530024	NM_001080495.3(TNRC18):c.5819G>T (p.Gly1940Val)	TNRC18 (G1940V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293506	NM_001080495.3(TNRC18):c.5816C>T (p.Pro1939Leu)	TNRC18 (P1939L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225106	NM_001080495.3(TNRC18):c.5780C>T (p.Ala1927Val)	TNRC18 (A1927V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180639	NM_001080495.3(TNRC18):c.5765G>A (p.Arg1922His)	TNRC18 (R1922H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391357	NM_001080495.3(TNRC18):c.5689C>T (p.Arg1897Trp)	TNRC18 (R1897W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277291	NM_001080495.3(TNRC18):c.5689C>G (p.Arg1897Gly)	TNRC18 (R1897G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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