"PreventionGenetics, part of Exact Sciences"[submitter] AND "FLT4"[gen - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042470	NM_182925.5(FLT4):c.4063G>A (p.Val1355Met)	FLT4 (V1355M)	Single nucleotide variant (missense variant)	FLT4-related disorder	GBenign
Select item 2634512	NM_182925.5(FLT4):c.4051C>T (p.Pro1351Ser)	FLT4 (P1351S)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 3030230	NM_182925.5(FLT4):c.4033G>A (p.Glu1345Lys)	FLT4 (E1345K)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 263059	NM_182925.5(FLT4):c.4005C>T (p.Ser1335=)	FLT4	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3032945	NM_182925.5(FLT4):c.3993G>A (p.Val1331=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 263057	NM_182925.5(FLT4):c.3971G>T (p.Arg1324Leu)	FLT4 (R1324L)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 263056	NM_182925.5(FLT4):c.3971G>C (p.Arg1324Pro)	FLT4 (R1324P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 263055	NM_182925.5(FLT4):c.3962G>A (p.Arg1321Gln)	FLT4 (R1321Q)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 263054	NM_182925.5(FLT4):c.3959G>A (p.Arg1320Gln)	FLT4 (R1320Q)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 263053	NM_182925.5(FLT4):c.3908G>C (p.Gly1303Ala)	FLT4 (G1303A)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3045605	NM_182925.5(FLT4):c.3885C>T (p.Ser1295=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 2632448	NM_182925.5(FLT4):c.3865A>C (p.Ser1289Arg)	FLT4 (S1289R)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 2635102	NM_182925.5(FLT4):c.3827G>A (p.Gly1276Glu)	FLT4 (G1276E)	Single nucleotide variant (missense variant)	FLT4-related disorder	GLikely pathogenic
Select item 3043868	NM_182925.5(FLT4):c.3825T>C (p.Ser1275=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 2636556	NM_182925.5(FLT4):c.3824_3825delinsTC (p.Ser1275Ile)	FLT4 (S1275I)	Indel (missense variant)	FLT4-related disorder	GUncertain significance
Select item 263052	NM_182925.5(FLT4):c.3807+34G>C	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 3048685	NM_182925.5(FLT4):c.3712G>T (p.Gly1238Trp)	FLT4 (G1238W)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 3029080	NM_182925.5(FLT4):c.3588G>A (p.Glu1196=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 3031890	NM_182925.5(FLT4):c.3571T>C (p.Ser1191Pro)	FLT4 (S1191P)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 263051	NM_182925.5(FLT4):c.3537+21G>A	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3035015	NM_182925.5(FLT4):c.3519C>G (p.Leu1173=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 263050	NM_182925.5(FLT4):c.3437G>A (p.Arg1146His)	FLT4 (R1146H)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 932061	NM_182925.5(FLT4):c.3410C>T (p.Pro1137Leu)	FLT4 (P1137L)	Single nucleotide variant (missense variant)	FLT4-related disorder +1 more	GLikely pathogenic
Select item 16266	NM_182925.5(FLT4):c.3257T>C (p.Ile1086Thr)	FLT4 (I1086T)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 263046	NM_182925.5(FLT4):c.3220-10G>T	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 263047	NM_182925.5(FLT4):c.3220-11T>C	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 263048	NM_182925.5(FLT4):c.3220-21A>C	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 263049	NM_182925.5(FLT4):c.3220-29A>G	FLT4	Single nucleotide variant (intron variant)	Hereditary lymphedema type I +3 more	GBenign
Select item 263045	NM_182925.5(FLT4):c.3219+37G>C	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 263044	NM_182925.5(FLT4):c.3198C>T (p.Pro1066=)	FLT4	Single nucleotide variant (synonymous variant)	Hereditary lymphedema type I +3 more	GBenign
Select item 3057532	NM_182925.5(FLT4):c.3186C>T (p.Ile1062=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 263043	NM_182925.5(FLT4):c.3147C>T (p.Asp1049=)	FLT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2636467	NM_182925.5(FLT4):c.3079T>C (p.Phe1027Leu)	FLT4 (F1027L)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 1297745	NM_182925.5(FLT4):c.3023C>T (p.Pro1008Leu)	FLT4 (P1008L)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2636940	NM_182925.5(FLT4):c.3019dup (p.Ser1007fs)	FLT4 (S1007fs)	Duplication (frameshift variant)	FLT4-related disorder	GPathogenic
Select item 263042	NM_182925.5(FLT4):c.3002-18C>A	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 263041	NM_182925.5(FLT4):c.3001+31T>G	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 698152	NM_182925.5(FLT4):c.2951G>A (p.Arg984Gln)	FLT4 (R984Q)	Single nucleotide variant (missense variant)	FLT4-related disorder +1 more	GLikely benign
Select item 16264	NM_182925.5(FLT4):c.2860C>T (p.Pro954Ser)	FLT4 (P954S)	Single nucleotide variant (missense variant)	Colorectal cancer +2 more	GBenign
Select item 2630521	NM_182925.5(FLT4):c.2815del (p.Leu939fs)	FLT4 (L939fs)	Deletion (frameshift variant)	FLT4-related disorder	GPathogenic
Select item 263040	NM_182925.5(FLT4):c.2761+44G>A	FLT4	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 3058494	NM_182925.5(FLT4):c.2739C>T (p.Leu913=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 263039	NM_182925.5(FLT4):c.2670C>G (p.His890Gln)	FLT4 (H890Q)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 3033514	NM_182925.5(FLT4):c.2658G>C (p.Thr886=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 263038	NM_182925.5(FLT4):c.2543-14C>T	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3056357	NM_182925.5(FLT4):c.2457C>G (p.Pro819=)	FLT4, LOC126807632	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 3053982	NM_182925.5(FLT4):c.2346C>T (p.Thr782=)	FLT4, LOC126807632	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 263036	NM_182925.5(FLT4):c.2299+13G>C	FLT4, LOC126807632	Single nucleotide variant (intron variant)	Hereditary lymphedema type I +2 more	GBenign
Select item 3061399	NM_182925.5(FLT4):c.2293G>A (p.Val765Met)	FLT4, LOC126807632 (V765M)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 3054395	NM_182925.5(FLT4):c.2235C>G (p.Arg745=)	FLT4, LOC126807632	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 263035	NM_182925.5(FLT4):c.2168-7C>G	FLT4, LOC126807632	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 263033	NM_182925.5(FLT4):c.2168-28A>G	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 263034	NM_182925.5(FLT4):c.2168-49G>A	FLT4	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 2632722	NM_182925.5(FLT4):c.2132_2134del (p.Trp711del)	FLT4 (W711del)	Deletion (inframe_deletion)	FLT4-related disorder	GUncertain significance
Select item 3052448	NM_182925.5(FLT4):c.2059C>G (p.Leu687Val)	FLT4 (L687V)	Single nucleotide variant (missense variant)	FLT4-related disorder	GBenign
Select item 2635972	NM_182925.5(FLT4):c.2059C>T (p.Leu687Phe)	FLT4 (L687F)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 3048702	NM_182925.5(FLT4):c.2049C>T (p.Asn683=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 2633187	NM_182925.5(FLT4):c.1925del (p.Arg642fs)	FLT4 (R642fs)	Deletion (frameshift variant)	FLT4-related disorder	GLikely pathogenic
Select item 263032	NM_182925.5(FLT4):c.1921C>T (p.Pro641Ser)	FLT4 (P641S)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 3052508	NM_182925.5(FLT4):c.1911C>G (p.Ser637Arg)	FLT4 (S637R)	Single nucleotide variant (missense variant)	FLT4-related disorder	GBenign
Select item 2636353	NM_182925.5(FLT4):c.1879G>A (p.Val627Met)	FLT4 (V627M)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 263031	NM_182925.5(FLT4):c.1815G>A (p.Pro605=)	FLT4	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3046561	NM_182925.5(FLT4):c.1710G>C (p.Glu570Asp)	FLT4 (E570D)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 3061693	NM_182925.5(FLT4):c.1689G>A (p.Lys563=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 263030	NM_182925.5(FLT4):c.1658-17T>G	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 2637203	NM_182925.5(FLT4):c.1614del (p.Asn538fs)	FLT4 (N538fs)	Deletion (frameshift variant)	FLT4-related disorder	GLikely pathogenic
Select item 263029	NM_182925.5(FLT4):c.1580A>G (p.Asn527Ser)	FLT4 (N527S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 263028	NM_182925.5(FLT4):c.1480A>G (p.Thr494Ala)	FLT4 (T494A)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 263027	NM_182925.5(FLT4):c.1422-10G>A	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 263026	NM_182925.5(FLT4):c.1421+37C>T	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 263025	NM_182925.5(FLT4):c.1421+19_1421+37del	FLT4	Deletion (intron variant)	not provided +1 more	GBenign
Select item 263024	NM_182925.5(FLT4):c.1344C>T (p.Tyr448=)	FLT4	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 263023	NM_182925.5(FLT4):c.1308G>A (p.Ser436=)	FLT4	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 263022	NM_182925.5(FLT4):c.1258+21C>T	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 263021	NM_182925.5(FLT4):c.1258+14G>A	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 2634525	NM_182925.5(FLT4):c.1179C>G (p.Ser393Arg)	FLT4 (S393R)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 3046938	NM_182925.5(FLT4):c.1130G>T (p.Gly377Val)	FLT4 (G377V)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 263020	NM_182925.5(FLT4):c.1104-42T>C	FLT4	Single nucleotide variant (intron variant)	Hereditary lymphedema type I +3 more	GBenign
Select item 263019	NM_182925.5(FLT4):c.1103+33A>C	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 263018	NM_182925.5(FLT4):c.1103+20A>G	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 263017	NM_182925.5(FLT4):c.1103+20A>C	FLT4	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 263016	NM_182925.5(FLT4):c.1103+18C>T	FLT4	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 263015	NM_182925.5(FLT4):c.1049A>T (p.Glu350Val)	FLT4 (E350V)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 3032061	NM_182925.5(FLT4):c.1032G>A (p.Glu344=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 2629137	NM_182925.5(FLT4):c.1003G>A (p.Val335Ile)	FLT4 (V335I)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 263072	NM_182925.5(FLT4):c.986-45C>T	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 3031287	NM_182925.5(FLT4):c.969C>T (p.Thr323=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 3047182	NM_182925.5(FLT4):c.897C>T (p.Asn299=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 3061439	NM_182925.5(FLT4):c.895A>C (p.Asn299His)	FLT4 (N299H)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 263071	NM_182925.5(FLT4):c.816+18G>C	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 2632446	NM_182925.5(FLT4):c.722A>G (p.Glu241Gly)	FLT4 (E241G)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 263069	NM_182925.5(FLT4):c.677-15T>C	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 263070	NM_182925.5(FLT4):c.677-28G>A	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 3032093	NM_182925.5(FLT4):c.676+6_676+30del	FLT4	Deletion (splice donor variant)	FLT4-related disorder	GLikely benign
Select item 263068	NM_182925.5(FLT4):c.676+18C>T	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 263067	NM_182925.5(FLT4):c.633A>G (p.Gly211=)	FLT4	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 2629109	NM_182925.5(FLT4):c.577G>A (p.Val193Met)	FLT4 (V193M)	Single nucleotide variant (missense variant)	FLT4-related disorder	GUncertain significance
Select item 3031493	NM_182925.5(FLT4):c.576C>T (p.Leu192=)	FLT4	Single nucleotide variant (synonymous variant)	FLT4-related disorder	GLikely benign
Select item 263064	NM_182925.5(FLT4):c.507G>T (p.Leu169=)	FLT4	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 263063	NM_182925.5(FLT4):c.489C>T (p.Pro163=)	FLT4	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign

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