CDC42BPG[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2334360	NM_017525.3(CDC42BPG):c.4580C>G (p.Pro1527Arg)	CDC42BPG (P1527R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490127	NM_017525.3(CDC42BPG):c.4510C>G (p.Pro1504Ala)	CDC42BPG (P1504A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379803	NM_017525.3(CDC42BPG):c.4465C>G (p.Arg1489Gly)	CDC42BPG (R1489G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264994	NM_017525.3(CDC42BPG):c.4453G>A (p.Glu1485Lys)	CDC42BPG (E1485K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265002	NM_017525.3(CDC42BPG):c.4409G>A (p.Arg1470Gln)	CDC42BPG (R1470Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322576	NM_017525.3(CDC42BPG):c.4384T>A (p.Ser1462Thr)	CDC42BPG (S1462T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214855	NM_017525.3(CDC42BPG):c.4360G>T (p.Gly1454Trp)	CDC42BPG (G1454W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217695	NM_017525.3(CDC42BPG):c.4334A>G (p.His1445Arg)	CDC42BPG (H1445R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140906	NM_017525.3(CDC42BPG):c.4322C>G (p.Thr1441Ser)	CDC42BPG (T1441S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513205	NM_017525.3(CDC42BPG):c.4289C>G (p.Pro1430Arg)	CDC42BPG (P1430R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617758	NM_017525.3(CDC42BPG):c.4240G>T (p.Val1414Leu)	CDC42BPG (V1414L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478949	NM_017525.3(CDC42BPG):c.4228T>G (p.Phe1410Val)	CDC42BPG (F1410V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482495	NM_017525.3(CDC42BPG):c.4217G>A (p.Ser1406Asn)	CDC42BPG (S1406N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265001	NM_017525.3(CDC42BPG):c.4187A>G (p.Asn1396Ser)	CDC42BPG (N1396S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491311	NM_017525.3(CDC42BPG):c.4183G>C (p.Asp1395His)	CDC42BPG (D1395H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301112	NM_017525.3(CDC42BPG):c.4177C>T (p.Leu1393Phe)	CDC42BPG (L1393F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456724	NM_017525.3(CDC42BPG):c.4138A>G (p.Asn1380Asp)	CDC42BPG (N1380D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140904	NM_017525.3(CDC42BPG):c.4096T>G (p.Phe1366Val)	CDC42BPG (F1366V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214533	NM_017525.3(CDC42BPG):c.4091C>A (p.Ser1364Tyr)	CDC42BPG (S1364Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384486	NM_017525.3(CDC42BPG):c.4082C>G (p.Pro1361Arg)	CDC42BPG (P1361R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140903	NM_017525.3(CDC42BPG):c.4057C>T (p.Leu1353Phe)	CDC42BPG (L1353F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259042	NM_017525.3(CDC42BPG):c.4051G>A (p.Val1351Met)	CDC42BPG (V1351M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551733	NM_017525.3(CDC42BPG):c.3931C>T (p.His1311Tyr)	CDC42BPG (H1311Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265004	NM_017525.3(CDC42BPG):c.3857G>A (p.Ser1286Asn)	CDC42BPG (S1286N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264991	NM_017525.3(CDC42BPG):c.3820G>A (p.Gly1274Arg)	CDC42BPG (G1274R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140902	NM_017525.3(CDC42BPG):c.3784G>A (p.Ala1262Thr)	CDC42BPG (A1262T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 717710	NM_017525.3(CDC42BPG):c.3771G>A (p.Pro1257=)	CDC42BPG	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3140901	NM_017525.3(CDC42BPG):c.3727G>A (p.Ala1243Thr)	CDC42BPG (A1243T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249044	NM_017525.3(CDC42BPG):c.3653G>A (p.Arg1218His)	CDC42BPG (R1218H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561043	NM_017525.3(CDC42BPG):c.3652C>T (p.Arg1218Cys)	CDC42BPG (R1218C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461133	NM_017525.3(CDC42BPG):c.3650G>A (p.Arg1217His)	CDC42BPG (R1217H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588221	NM_017525.3(CDC42BPG):c.3649C>T (p.Arg1217Cys)	CDC42BPG (R1217C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140900	NM_017525.3(CDC42BPG):c.3643T>C (p.Trp1215Arg)	CDC42BPG (W1215R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314643	NM_017525.3(CDC42BPG):c.3631G>A (p.Gly1211Ser)	CDC42BPG (G1211S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515918	NM_017525.3(CDC42BPG):c.3595G>A (p.Val1199Ile)	CDC42BPG (V1199I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393804	NM_017525.3(CDC42BPG):c.3578C>T (p.Pro1193Leu)	CDC42BPG (P1193L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350410	NM_017525.3(CDC42BPG):c.3571C>G (p.Arg1191Gly)	CDC42BPG (R1191G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140899	NM_017525.3(CDC42BPG):c.3536G>A (p.Cys1179Tyr)	CDC42BPG (C1179Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140898	NM_017525.3(CDC42BPG):c.3529C>G (p.Arg1177Gly)	CDC42BPG (R1177G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300882	NM_017525.3(CDC42BPG):c.3446G>A (p.Cys1149Tyr)	CDC42BPG (C1149Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641935	NM_017525.3(CDC42BPG):c.3366C>T (p.Asn1122=)	CDC42BPG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2328146	NM_017525.3(CDC42BPG):c.3359G>A (p.Arg1120His)	CDC42BPG (R1120H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140896	NM_017525.3(CDC42BPG):c.3292G>A (p.Ala1098Thr)	CDC42BPG (A1098T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509073	NM_017525.3(CDC42BPG):c.3232G>A (p.Val1078Met)	CDC42BPG (V1078M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523507	NM_017525.3(CDC42BPG):c.3226C>T (p.Arg1076Trp)	CDC42BPG (R1076W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264992	NM_017525.3(CDC42BPG):c.3214C>T (p.Arg1072Trp)	CDC42BPG (R1072W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140895	NM_017525.3(CDC42BPG):c.3212C>T (p.Ala1071Val)	CDC42BPG (A1071V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219438	NM_017525.3(CDC42BPG):c.3167G>A (p.Arg1056His)	CDC42BPG (R1056H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140894	NM_017525.3(CDC42BPG):c.3166C>T (p.Arg1056Cys)	CDC42BPG (R1056C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384216	NM_017525.3(CDC42BPG):c.3140T>G (p.Leu1047Arg)	CDC42BPG (L1047R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518289	NM_017525.3(CDC42BPG):c.3122C>T (p.Thr1041Met)	CDC42BPG (T1041M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262499	NM_017525.3(CDC42BPG):c.3112C>G (p.Pro1038Ala)	CDC42BPG (P1038A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251919	NM_017525.3(CDC42BPG):c.3086G>A (p.Arg1029Lys)	CDC42BPG (R1029K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318831	NM_017525.3(CDC42BPG):c.3045T>A (p.Asp1015Glu)	CDC42BPG (D1015E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284918	NM_017525.3(CDC42BPG):c.3038C>T (p.Ala1013Val)	CDC42BPG (A1013V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390156	NM_017525.3(CDC42BPG):c.3011C>T (p.Pro1004Leu)	CDC42BPG (P1004L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208573	NM_017525.3(CDC42BPG):c.2969C>T (p.Pro990Leu)	CDC42BPG (P990L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408548	NM_017525.3(CDC42BPG):c.2960G>C (p.Arg987Thr)	CDC42BPG (R987T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401024	NM_017525.3(CDC42BPG):c.2905G>A (p.Val969Met)	CDC42BPG (V969M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456317	NM_017525.3(CDC42BPG):c.2827G>A (p.Glu943Lys)	CDC42BPG (E943K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312079	NM_017525.3(CDC42BPG):c.2804G>A (p.Arg935His)	CDC42BPG (R935H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3264995	NM_017525.3(CDC42BPG):c.2803C>T (p.Arg935Cys)	CDC42BPG (R935C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268738	NM_017525.3(CDC42BPG):c.2798T>A (p.Leu933His)	CDC42BPG (L933H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268737	NM_017525.3(CDC42BPG):c.2797C>G (p.Leu933Val)	CDC42BPG (L933V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529853	NM_017525.3(CDC42BPG):c.2767C>G (p.Gln923Glu)	CDC42BPG (Q923E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550365	NM_017525.3(CDC42BPG):c.2747G>A (p.Cys916Tyr)	CDC42BPG (C916Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204425	NM_017525.3(CDC42BPG):c.2737G>A (p.Gly913Ser)	CDC42BPG (G913S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465104	NM_017525.3(CDC42BPG):c.2728G>C (p.Asp910His)	CDC42BPG (D910H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140892	NM_017525.3(CDC42BPG):c.2701G>A (p.Gly901Ser)	CDC42BPG (G901S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264999	NM_017525.3(CDC42BPG):c.2690C>T (p.Ser897Leu)	CDC42BPG (S897L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265009	NM_017525.3(CDC42BPG):c.2666C>T (p.Pro889Leu)	CDC42BPG (P889L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516361	NM_017525.3(CDC42BPG):c.2651G>A (p.Arg884Gln)	CDC42BPG (R884Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364696	NM_017525.3(CDC42BPG):c.2644C>T (p.Arg882Cys)	CDC42BPG (R882C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140891	NM_017525.3(CDC42BPG):c.2642T>C (p.Leu881Pro)	CDC42BPG (L881P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140890	NM_017525.3(CDC42BPG):c.2639C>T (p.Thr880Met)	CDC42BPG (T880M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140889	NM_017525.3(CDC42BPG):c.2637C>A (p.His879Gln)	CDC42BPG (H879Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140888	NM_017525.3(CDC42BPG):c.2632T>G (p.Ser878Ala)	CDC42BPG (S878A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264998	NM_017525.3(CDC42BPG):c.2582C>T (p.Ala861Val)	CDC42BPG (A861V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140887	NM_017525.3(CDC42BPG):c.2562G>A (p.Met854Ile)	CDC42BPG (M854I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466809	NM_017525.3(CDC42BPG):c.2560A>G (p.Met854Val)	CDC42BPG (M854V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307611	NM_017525.3(CDC42BPG):c.2553C>G (p.Ser851Arg)	CDC42BPG (S851R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386272	NM_017525.3(CDC42BPG):c.2537C>T (p.Pro846Leu)	CDC42BPG (P846L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298381	NM_017525.3(CDC42BPG):c.2531T>A (p.Leu844Gln)	CDC42BPG (L844Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265006	NM_017525.3(CDC42BPG):c.2524C>A (p.Pro842Thr)	CDC42BPG (P842T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373029	NM_017525.3(CDC42BPG):c.2513A>G (p.His838Arg)	CDC42BPG (H838R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264990	NM_017525.3(CDC42BPG):c.2459G>A (p.Ser820Asn)	CDC42BPG (S820N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140886	NM_017525.3(CDC42BPG):c.2423C>G (p.Pro808Arg)	CDC42BPG (P808R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623057	NM_017525.3(CDC42BPG):c.2404G>A (p.Gly802Arg)	CDC42BPG (G802R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208703	NM_017525.3(CDC42BPG):c.2396G>A (p.Arg799Gln)	CDC42BPG (R799Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272188	NM_017525.3(CDC42BPG):c.2374G>A (p.Ala792Thr)	CDC42BPG (A792T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2600875	NM_017525.3(CDC42BPG):c.2210T>C (p.Met737Thr)	CDC42BPG (M737T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140885	NM_017525.3(CDC42BPG):c.2168G>A (p.Arg723Gln)	CDC42BPG (R723Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140884	NM_017525.3(CDC42BPG):c.2047G>T (p.Asp683Tyr)	CDC42BPG (D683Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229770	NM_017525.3(CDC42BPG):c.2044G>A (p.Ala682Thr)	CDC42BPG (A682T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641936	NM_017525.3(CDC42BPG):c.2019G>A (p.Thr673=)	CDC42BPG	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3140883	NM_017525.3(CDC42BPG):c.2015A>C (p.Glu672Ala)	CDC42BPG (E672A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362971	NM_017525.3(CDC42BPG):c.2011C>T (p.Arg671Trp)	CDC42BPG (R671W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358850	NM_017525.3(CDC42BPG):c.2009G>A (p.Arg670Gln)	CDC42BPG (R670Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345703	NM_017525.3(CDC42BPG):c.1940G>A (p.Arg647Gln)	CDC42BPG (R647Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2233020	NM_017525.3(CDC42BPG):c.1937G>T (p.Ser646Ile)	CDC42BPG (S646I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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