ClinVar for Gene (Select 2324) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065289	NM_182925.5(FLT4):c.677-3C>T	FLT4	Single nucleotide variant (intron variant)	Hereditary lymphedema type I	GUncertain significance
Select item 3064021	NM_182925.5(FLT4):c.2765C>T (p.Pro922Leu)	FLT4 (P922L)	Single nucleotide variant (missense variant)	Congenital heart defects, multiple types, 7	GUncertain significance
Select item 3062850	GRCh37/hg19 5q35.3(chr5:177944162-180183615)x3	ADAMTS2, C5orf60 +27 more	Copy number gain	not specified	GUncertain significance
Select item 3062813	GRCh37/hg19 5q35.3(chr5:177944162-180198875)x3	ZNF354A, ZNF354B +27 more	Copy number gain	not specified	GPathogenic
Select item 3062295	NM_182925.5(FLT4):c.2922_2941del (p.Gly975fs)	FLT4 (G975fs)	Deletion (frameshift variant)	Congenital heart defects, multiple types, 7	GLikely pathogenic
Select item 3061693	NM_182925.5(FLT4):c.1689G>A (p.Lys563=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3061439	NM_182925.5(FLT4):c.895A>C (p.Asn299His)	FLT4 (N299H)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 3061399	NM_182925.5(FLT4):c.2293G>A (p.Val765Met)	FLT4, LOC126807632 (V765M)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 3058494	NM_182925.5(FLT4):c.2739C>T (p.Leu913=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3057532	NM_182925.5(FLT4):c.3186C>T (p.Ile1062=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3056357	NM_182925.5(FLT4):c.2457C>G (p.Pro819=)	FLT4, LOC126807632	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3054395	NM_182925.5(FLT4):c.2235C>G (p.Arg745=)	FLT4, LOC126807632	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3053982	NM_182925.5(FLT4):c.2346C>T (p.Thr782=)	FLT4, LOC126807632	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3052508	NM_182925.5(FLT4):c.1911C>G (p.Ser637Arg)	FLT4 (S637R)	Single nucleotide variant (missense variant)	FLT4-related condition	GBenign
Select item 3052448	NM_182925.5(FLT4):c.2059C>G (p.Leu687Val)	FLT4 (L687V)	Single nucleotide variant (missense variant)	FLT4-related condition	GBenign
Select item 3048702	NM_182925.5(FLT4):c.2049C>T (p.Asn683=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3048685	NM_182925.5(FLT4):c.3712G>T (p.Gly1238Trp)	FLT4 (G1238W)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 3047195	NM_182925.5(FLT4):c.435G>A (p.Thr145=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3047182	NM_182925.5(FLT4):c.897C>T (p.Asn299=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3046938	NM_182925.5(FLT4):c.1130G>T (p.Gly377Val)	FLT4 (G377V)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 3046561	NM_182925.5(FLT4):c.1710G>C (p.Glu570Asp)	FLT4 (E570D)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 3045605	NM_182925.5(FLT4):c.3885C>T (p.Ser1295=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3045299	NM_182925.5(FLT4):c.226G>A (p.Glu76Lys)	FLT4 (E76K)	Single nucleotide variant (missense variant)	FLT4-related condition	GLikely benign
Select item 3043868	NM_182925.5(FLT4):c.3825T>C (p.Ser1275=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3042470	NM_182925.5(FLT4):c.4063G>A (p.Val1355Met)	FLT4 (V1355M)	Single nucleotide variant (missense variant)	FLT4-related condition	GBenign
Select item 3035015	NM_182925.5(FLT4):c.3519C>G (p.Leu1173=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3033514	NM_182925.5(FLT4):c.2658G>C (p.Thr886=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3032945	NM_182925.5(FLT4):c.3993G>A (p.Val1331=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3032093	NM_182925.5(FLT4):c.676+6_676+30del	FLT4	Deletion (splice donor variant)	FLT4-related condition	GLikely benign
Select item 3032061	NM_182925.5(FLT4):c.1032G>A (p.Glu344=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3031890	NM_182925.5(FLT4):c.3571T>C (p.Ser1191Pro)	FLT4 (S1191P)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 3031493	NM_182925.5(FLT4):c.576C>T (p.Leu192=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3031287	NM_182925.5(FLT4):c.969C>T (p.Thr323=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3030230	NM_182925.5(FLT4):c.4033G>A (p.Glu1345Lys)	FLT4 (E1345K)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 3029080	NM_182925.5(FLT4):c.3588G>A (p.Glu1196=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related condition	GLikely benign
Select item 3027331	NM_182925.5(FLT4):c.1534G>A (p.Glu512Lys)	FLT4 (E512K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3026009	NM_182925.5(FLT4):c.2292C>T (p.Ala764=)	FLT4, LOC126807632	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2695390	NM_182925.5(FLT4):c.1657+5G>C	FLT4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2689081	NM_182925.5(FLT4):c.3977C>T (p.Ala1326Val)	FLT4 (A1326V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2689080	NM_182925.5(FLT4):c.2644A>G (p.Lys882Glu)	FLT4 (K882E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2684438	GRCh37/hg19 5q35.3(chr5:179565253-180051586)x3	CNOT6, FLT4 +4 more	Copy number gain	not provided	GUncertain significance
Select item 2684436	GRCh37/hg19 5q35.3(chr5:178581633-180719789)x3	ADAMTS2, BTNL3 +34 more	Copy number gain	not provided	GUncertain significance
Select item 2673040	NM_182925.5(FLT4):c.1740C>A (p.Ala580=)	FLT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2672120	NM_182925.5(FLT4):c.1519T>C (p.Trp507Arg)	FLT4 (W507R)	Single nucleotide variant (missense variant)	Hereditary lymphedema type I	GUncertain significance
Select item 2664279	NM_182925.5(FLT4):c.3109G>A (p.Asp1037Asn)	FLT4 (D1037N)	Single nucleotide variant (missense variant)	Hereditary lymphedema type I	GPathogenic
Select item 2664278	NM_182925.5(FLT4):c.2771T>A (p.Met924Lys)	FLT4 (M924K)	Single nucleotide variant (missense variant)	Hereditary lymphedema type I	GPathogenic
Select item 2664275	NM_182925.5(FLT4):c.2717_2734dup (p.Asn911_Leu912insHisLeuAsnValValAsn)	FLT4	Duplication (inframe_insertion)	Hereditary lymphedema type I	GLikely pathogenic
Select item 2656158	NM_182925.5(FLT4):c.1491C>T (p.Ala497=)	FLT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656157	NM_182925.5(FLT4):c.1525G>A (p.Glu509Lys)	FLT4 (E509K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656156	NM_182925.5(FLT4):c.2055C>A (p.Thr685=)	FLT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656155	NM_182925.5(FLT4):c.3002C>T (p.Ala1001Val)	FLT4 (A1001V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656154	NM_182925.5(FLT4):c.3145G>A (p.Asp1049Asn)	FLT4 (D1049N)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2656153	NM_182925.5(FLT4):c.3525C>A (p.Gly1175=)	FLT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656152	NM_182925.5(FLT4):c.3532C>T (p.Leu1178=)	FLT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656151	NM_182925.5(FLT4):c.3893+131G>A	FLT4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2637203	NM_182925.5(FLT4):c.1614del (p.Asn538fs)	FLT4 (N538fs)	Deletion (frameshift variant)	FLT4-related condition	GLikely pathogenic
Select item 2636940	NM_182925.5(FLT4):c.3019dup (p.Ser1007fs)	FLT4 (S1007fs)	Duplication (frameshift variant)	FLT4-related condition	GPathogenic
Select item 2636879	NM_182925.5(FLT4):c.89C>T (p.Pro30Leu)	FLT4 (P30L)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2636556	NM_182925.5(FLT4):c.3824_3825delinsTC (p.Ser1275Ile)	FLT4 (S1275I)	Indel (missense variant)	FLT4-related condition	GUncertain significance
Select item 2636540	NM_182925.5(FLT4):c.400G>A (p.Asp134Asn)	FLT4 (D134N)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2636467	NM_182925.5(FLT4):c.3079T>C (p.Phe1027Leu)	FLT4 (F1027L)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2636353	NM_182925.5(FLT4):c.1879G>A (p.Val627Met)	FLT4 (V627M)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2635972	NM_182925.5(FLT4):c.2059C>T (p.Leu687Phe)	FLT4 (L687F)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2635102	NM_182925.5(FLT4):c.3827G>A (p.Gly1276Glu)	FLT4 (G1276E)	Single nucleotide variant (missense variant)	FLT4-related condition	GLikely pathogenic
Select item 2634525	NM_182925.5(FLT4):c.1179C>G (p.Ser393Arg)	FLT4 (S393R)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2634512	NM_182925.5(FLT4):c.4051C>T (p.Pro1351Ser)	FLT4 (P1351S)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2633187	NM_182925.5(FLT4):c.1925del (p.Arg642fs)	FLT4 (R642fs)	Deletion (frameshift variant)	FLT4-related condition	GLikely pathogenic
Select item 2632722	NM_182925.5(FLT4):c.2132_2134del (p.Trp711del)	FLT4 (W711del)	Deletion (inframe_deletion)	FLT4-related condition	GUncertain significance
Select item 2632448	NM_182925.5(FLT4):c.3865A>C (p.Ser1289Arg)	FLT4 (S1289R)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2632446	NM_182925.5(FLT4):c.722A>G (p.Glu241Gly)	FLT4 (E241G)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2631647	NM_182925.5(FLT4):c.482C>A (p.Ser161Tyr)	FLT4 (S161Y)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2630521	NM_182925.5(FLT4):c.2815del (p.Leu939fs)	FLT4 (L939fs)	Deletion (frameshift variant)	FLT4-related condition	GPathogenic
Select item 2629137	NM_182925.5(FLT4):c.1003G>A (p.Val335Ile)	FLT4 (V335I)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2629109	NM_182925.5(FLT4):c.577G>A (p.Val193Met)	FLT4 (V193M)	Single nucleotide variant (missense variant)	FLT4-related condition	GUncertain significance
Select item 2620864	NM_182925.5(FLT4):c.3156G>T (p.Lys1052Asn)	FLT4 (K1052N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2618846	NM_182925.5(FLT4):c.2651G>A (p.Gly884Asp)	FLT4 (G884D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2604386	NM_182925.5(FLT4):c.2105C>G (p.Ala702Gly)	FLT4 (A702G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2592701	NM_182925.5(FLT4):c.3653C>T (p.Pro1218Leu)	FLT4 (P1218L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2578991	NM_182925.5(FLT4):c.2491C>T (p.Leu831=)	FLT4, LOC126807632	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2562460	NM_182925.5(FLT4):c.3813C>G (p.Asn1271Lys)	FLT4 (N1271K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2520989	NM_182925.5(FLT4):c.3566G>A (p.Arg1189His)	FLT4 (R1189H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517396	NM_182925.5(FLT4):c.2896C>T (p.Leu966Phe)	FLT4 (L966F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2509031	NM_182925.5(FLT4):c.3469A>C (p.Lys1157Gln)	FLT4 (K1157Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2505672	NM_182925.5(FLT4):c.265G>A (p.Ala89Thr)	FLT4 (A89T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2505647	NM_182925.5(FLT4):c.1459C>G (p.Arg487Gly)	FLT4 (R487G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2503331	NM_182925.5(FLT4):c.2684C>T (p.Ser895Leu)	FLT4 (S895L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2502491	NM_182925.5(FLT4):c.238G>C (p.Val80Leu)	FLT4 (V80L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2502010	NM_182925.5(FLT4):c.4079ACA[1] (p.Asn1361del)	FLT4 (N1361del)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 2501818	NM_182925.5(FLT4):c.3179G>A (p.Arg1060Gln)	FLT4 (R1060Q)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 2500428	NM_182925.5(FLT4):c.3289G>A (p.Val1097Met)	FLT4 (V1097M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2498995	NM_182925.5(FLT4):c.3808-127G>C	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2498270	NM_182925.5(FLT4):c.124G>A (p.Asp42Asn)	FLT4 (D42N)	Single nucleotide variant (missense variant)	Teratoma	GUncertain significance
Select item 2468053	NM_182925.5(FLT4):c.3556A>G (p.Met1186Val)	FLT4 (M1186V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2458980	NM_182925.5(FLT4):c.328G>A (p.Val110Ile)	FLT4 (V110I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2457640	NM_182925.5(FLT4):c.14C>G (p.Ala5Gly)	FLT4 (A5G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2446283	NM_182925.5(FLT4):c.251G>A (p.Cys84Tyr)	FLT4 (C84Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2445224	NM_182925.5(FLT4):c.3332G>A (p.Gly1111Glu)	FLT4 (G1111E)	Single nucleotide variant (missense variant)	Hereditary lymphedema type I	GPathogenic
Select item 2443468	NM_182925.5(FLT4):c.3824G>C (p.Ser1275Thr)	FLT4 (S1275T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2442714	NM_182925.5(FLT4):c.1933C>A (p.Pro645Thr)	FLT4 (P645T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2441699	NM_182925.5(FLT4):c.1104-2A>G	FLT4	Single nucleotide variant (splice acceptor variant)	Hereditary lymphedema type I	GUncertain significance

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