30025[HGNC] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57116	GRCh38/hg38 10q23.33-25.3(chr10:95112607-116776637)x3	LOC130004500, LOC130004501 +821 more	Copy number gain	See cases	GPathogenic
Select item 59707	GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3	EDRF1-AS1, EDRF1-DT +1036 more	Copy number gain	See cases	GPathogenic
Select item 148679	GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3	GSTO1, GSTO2 +1097 more	Copy number gain	See cases	GPathogenic
Select item 2379759	NM_015062.5(PPRC1):c.7G>T (p.Ala3Ser)	LOC130004585, PPRC1 (A3S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455915	NM_015062.5(PPRC1):c.14G>T (p.Arg5Leu)	LOC130004585, PPRC1 (R5L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3043437	NM_015062.5(PPRC1):c.19C>A (p.Arg7=)	LOC130004585, PPRC1	Single nucleotide variant (synonymous variant +1 more)	PPRC1-related disorder	GLikely benign
Select item 2640776	NM_015062.5(PPRC1):c.24A>G (p.Arg8=)	LOC130004585, PPRC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3217953	NM_015062.5(PPRC1):c.35C>T (p.Ala12Val)	LOC130004585, PPRC1 (A12V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2561980	NM_015062.5(PPRC1):c.47G>A (p.Ser16Asn)	LOC130004585, PPRC1 (S16N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543725	NM_015062.5(PPRC1):c.49G>C (p.Gly17Arg)	LOC130004585, PPRC1 (G17R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295784	NM_015062.5(PPRC1):c.61C>G (p.Pro21Ala)	LOC130004585, LOC130004586 +1 more (P21A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3217968	NM_015062.5(PPRC1):c.77G>C (p.Gly26Ala)	LOC130004586, PPRC1 (G26A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295785	NM_015062.5(PPRC1):c.95G>T (p.Trp32Leu)	LOC130004586, PPRC1 (W32L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254828	NM_015062.5(PPRC1):c.125C>T (p.Thr42Ile)	LOC130004586, PPRC1 (T42I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468322	NM_015062.5(PPRC1):c.133G>A (p.Ala45Thr)	LOC130004586, PPRC1 (A45T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3217935	NM_015062.5(PPRC1):c.173C>T (p.Ala58Val)	PPRC1 (A58V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406233	NM_015062.5(PPRC1):c.176G>A (p.Gly59Asp)	PPRC1 (G59D)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3217940	NM_015062.5(PPRC1):c.227A>G (p.Lys76Arg)	PPRC1 (K76R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2640777	NM_015062.5(PPRC1):c.247C>T (p.Leu83=)	PPRC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3040796	NM_015062.5(PPRC1):c.253C>T (p.Leu85=)	PPRC1	Single nucleotide variant (synonymous variant +1 more)	PPRC1-related disorder	GLikely benign
Select item 2486476	NM_015062.5(PPRC1):c.257A>C (p.Gln86Pro)	PPRC1 (Q86P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309602	NM_015062.5(PPRC1):c.316A>T (p.Ile106Phe)	PPRC1 (I106F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316877	NM_015062.5(PPRC1):c.395C>T (p.Thr132Met)	LOC126861022, PPRC1 (T132M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545222	NM_015062.5(PPRC1):c.417T>A (p.Asp139Glu)	LOC126861022, PPRC1 (D139E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548557	NM_015062.5(PPRC1):c.508C>T (p.Leu170Phe)	LOC126861022, PPRC1 (L50F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217966	NM_015062.5(PPRC1):c.515G>A (p.Arg172Gln)	LOC126861022, PPRC1 (R52Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467549	NM_015062.5(PPRC1):c.566G>A (p.Ser189Asn)	LOC126861022, PPRC1 (S69N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640778	NM_015062.5(PPRC1):c.624C>T (p.Asp208=)	LOC126861022, PPRC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3309595	NM_015062.5(PPRC1):c.645A>T (p.Leu215Phe)	LOC126861022, PPRC1 (L215F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217967	NM_015062.5(PPRC1):c.721C>G (p.Gln241Glu)	LOC126861022, PPRC1 (Q121E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335504	NM_015062.5(PPRC1):c.784G>A (p.Gly262Arg)	LOC126861022, PPRC1 (G142R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537755	NM_015062.5(PPRC1):c.827T>G (p.Met276Arg)	LOC126861022, PPRC1 (M276R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3033278	NM_015062.5(PPRC1):c.859G>C (p.Ala287Pro)	LOC126861022, PPRC1 (A167P +1 more)	Single nucleotide variant (missense variant)	PPRC1-related disorder	GBenign
Select item 3217969	NM_015062.5(PPRC1):c.889G>A (p.Ala297Thr)	LOC126861022, PPRC1 (A177T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309600	NM_015062.5(PPRC1):c.901A>G (p.Ser301Gly)	LOC126861022, PPRC1 (S301G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161691	NM_015062.5(PPRC1):c.904A>G (p.Ile302Val)	LOC126861022, PPRC1 (I302V +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance
Select item 2369237	NM_015062.5(PPRC1):c.956A>G (p.Asn319Ser)	PPRC1 (N199S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380917	NM_015062.5(PPRC1):c.1013C>T (p.Thr338Ile)	PPRC1 (T218I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347592	NM_015062.5(PPRC1):c.1069G>A (p.Asp357Asn)	PPRC1 (D237N +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3217930	NM_015062.5(PPRC1):c.1096C>G (p.Arg366Gly)	PPRC1 (R366G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211613	NM_015062.5(PPRC1):c.1097G>A (p.Arg366Gln)	PPRC1 (R366Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205629	NM_015062.5(PPRC1):c.1126C>T (p.Leu376Phe)	PPRC1 (L256F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3047648	NM_015062.5(PPRC1):c.1239G>C (p.Gly413=)	PPRC1	Single nucleotide variant (synonymous variant)	PPRC1-related disorder	GLikely benign
Select item 3217931	NM_015062.5(PPRC1):c.1241T>C (p.Leu414Ser)	PPRC1 (L294S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3057402	NM_015062.5(PPRC1):c.1257G>A (p.Glu419=)	PPRC1	Single nucleotide variant (synonymous variant)	PPRC1-related disorder	GLikely benign
Select item 3217932	NM_015062.5(PPRC1):c.1271C>T (p.Ser424Leu)	PPRC1 (S304L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309592	NM_015062.5(PPRC1):c.1351C>A (p.Pro451Thr)	PPRC1 (P331T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304976	NM_015062.5(PPRC1):c.1352C>T (p.Pro451Leu)	PPRC1 (P451L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2640779	NM_015062.5(PPRC1):c.1394A>G (p.Lys465Arg)	PPRC1 (K345R +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3217933	NM_015062.5(PPRC1):c.1429A>G (p.Arg477Gly)	PPRC1 (R357G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407720	NM_015062.5(PPRC1):c.1451G>A (p.Arg484His)	PPRC1 (R484H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464549	NM_015062.5(PPRC1):c.1453G>A (p.Gly485Arg)	PPRC1 (G485R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543971	NM_015062.5(PPRC1):c.1562C>T (p.Pro521Leu)	PPRC1 (P401L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217934	NM_015062.5(PPRC1):c.1582T>A (p.Trp528Arg)	PPRC1 (W408R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3057089	NM_015062.5(PPRC1):c.1606A>G (p.Ser536Gly)	PPRC1 (S416G +1 more)	Single nucleotide variant (missense variant)	PPRC1-related disorder	GBenign
Select item 2412564	NM_015062.5(PPRC1):c.1705C>T (p.Pro569Ser)	PPRC1 (P569S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309603	NM_015062.5(PPRC1):c.1813G>C (p.Val605Leu)	PPRC1 (V485L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309596	NM_015062.5(PPRC1):c.1820T>G (p.Val607Gly)	PPRC1 (V487G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232434	NM_015062.5(PPRC1):c.1824C>G (p.Asp608Glu)	PPRC1 (D488E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2689822	NM_015062.5(PPRC1):c.1825C>T (p.Pro609Ser)	PPRC1 (P489S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2463946	NM_015062.5(PPRC1):c.1835T>C (p.Val612Ala)	PPRC1 (V612A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217936	NM_015062.5(PPRC1):c.1849A>G (p.Thr617Ala)	PPRC1 (T617A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2593051	NM_015062.5(PPRC1):c.1870C>T (p.Pro624Ser)	PPRC1 (P624S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640780	NM_015062.5(PPRC1):c.1878G>A (p.Pro626=)	PPRC1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2553927	NM_015062.5(PPRC1):c.1888G>T (p.Val630Leu)	PPRC1 (V630L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309594	NM_015062.5(PPRC1):c.1975G>A (p.Val659Ile)	PPRC1 (V539I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293127	NM_015062.5(PPRC1):c.1978C>T (p.Pro660Ser)	PPRC1 (P540S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217937	NM_015062.5(PPRC1):c.1988C>T (p.Pro663Leu)	PPRC1 (P543L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217938	NM_015062.5(PPRC1):c.2086G>A (p.Gly696Ser)	PPRC1 (G576S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278710	NM_015062.5(PPRC1):c.2185G>A (p.Val729Ile)	PPRC1 (V729I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309586	NM_015062.5(PPRC1):c.2203A>T (p.Ile735Phe)	PPRC1 (I615F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217939	NM_015062.5(PPRC1):c.2243C>T (p.Pro748Leu)	PPRC1 (P628L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347815	NM_015062.5(PPRC1):c.2248C>A (p.Pro750Thr)	PPRC1 (P630T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3060162	NM_015062.5(PPRC1):c.2279_2290dup (p.Arg763_Gln764insArgGlnGlnArg)	PPRC1	Duplication	PPRC1-related disorder	GBenign
Select item 3309589	NM_015062.5(PPRC1):c.2402C>G (p.Pro801Arg)	PPRC1 (P681R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365197	NM_015062.5(PPRC1):c.2437A>T (p.Thr813Ser)	PPRC1 (T693S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3056952	NM_015062.5(PPRC1):c.2464G>A (p.Val822Ile)	PPRC1 (V702I +1 more)	Single nucleotide variant (missense variant)	PPRC1-related disorder	GBenign
Select item 3055463	NM_015062.5(PPRC1):c.2501C>G (p.Pro834Arg)	PPRC1 (P714R +1 more)	Single nucleotide variant (missense variant)	PPRC1-related disorder	GLikely benign
Select item 2288765	NM_015062.5(PPRC1):c.2503G>A (p.Val835Ile)	PPRC1 (V715I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217941	NM_015062.5(PPRC1):c.2522C>T (p.Ser841Leu)	PPRC1 (S721L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217942	NM_015062.5(PPRC1):c.2563T>G (p.Leu855Val)	PPRC1 (L735V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529042	NM_015062.5(PPRC1):c.2572C>A (p.Pro858Thr)	PPRC1 (P738T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478285	NM_015062.5(PPRC1):c.2589G>T (p.Gln863His)	PPRC1 (Q863H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217943	NM_015062.5(PPRC1):c.2611A>C (p.Thr871Pro)	PPRC1 (T751P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309599	NM_015062.5(PPRC1):c.2614C>A (p.Pro872Thr)	PPRC1 (P872T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491345	NM_015062.5(PPRC1):c.2621C>T (p.Ser874Leu)	PPRC1 (S754L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3038036	NM_015062.5(PPRC1):c.2624T>C (p.Met875Thr)	PPRC1 (M755T +1 more)	Single nucleotide variant (missense variant)	PPRC1-related disorder	GLikely benign
Select item 2347393	NM_015062.5(PPRC1):c.2681C>T (p.Pro894Leu)	PPRC1 (P774L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3033715	NM_015062.5(PPRC1):c.2726T>C (p.Val909Ala)	PPRC1 (V789A +1 more)	Single nucleotide variant (missense variant)	PPRC1-related disorder	GBenign
Select item 2631643	NM_015062.5(PPRC1):c.2729T>C (p.Leu910Pro)	PPRC1 (L790P +1 more)	Single nucleotide variant (missense variant)	PPRC1-related disorder	GUncertain significance
Select item 3217944	NM_015062.5(PPRC1):c.2750A>C (p.Tyr917Ser)	PPRC1 (Y917S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217945	NM_015062.5(PPRC1):c.2813C>G (p.Pro938Arg)	PPRC1 (P818R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291625	NM_015062.5(PPRC1):c.2815C>T (p.Pro939Ser)	PPRC1 (P939S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217946	NM_015062.5(PPRC1):c.2816C>G (p.Pro939Arg)	PPRC1 (P819R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555354	NM_015062.5(PPRC1):c.2816C>T (p.Pro939Leu)	PPRC1 (P819L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534136	NM_015062.5(PPRC1):c.2818C>G (p.Pro940Ala)	PPRC1 (P940A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217947	NM_015062.5(PPRC1):c.2821C>T (p.Pro941Ser)	PPRC1 (P941S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556760	NM_015062.5(PPRC1):c.2825C>T (p.Thr942Met)	PPRC1 (T942M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454672	NM_015062.5(PPRC1):c.2830C>T (p.Pro944Ser)	PPRC1 (P824S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336652	NM_015062.5(PPRC1):c.2849C>T (p.Pro950Leu)	PPRC1 (P830L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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