"GeneDx"[submitter] AND "FLT4"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58118	GRCh38/hg38 5q32-35.3(chr5:149714592-181272151)x3	LOC132089226, LOC132089227 +1167 more	Copy number gain	See cases	GPathogenic
Select item 58123	GRCh38/hg38 5q35.2-35.3(chr5:175889986-180793986)x3	ADAMTS2, ARL10 +292 more	Copy number gain	See cases	GPathogenic
Select item 145959	GRCh38/hg38 5q35.3(chr5:179669736-180897169)x1	CANX, CBY3 +85 more	Copy number loss	See cases	GLikely pathogenic
Select item 1274028	NM_182925.5(FLT4):c.*60G>A	FLT4	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 2502010	NM_182925.5(FLT4):c.4079ACA[1] (p.Asn1361del)	FLT4 (N1361del)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 1300689	NM_182925.5(FLT4):c.3999C>A (p.Tyr1333Ter)	FLT4 (Y1333*)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic
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 1279900	NM_182925.5(FLT4):c.3893+621G>A	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252124	NM_182925.5(FLT4):c.3893+464G>A	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268187	NM_182925.5(FLT4):c.3893+176G>A	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3377884	NM_182925.5(FLT4):c.3870G>C (p.Arg1290Ser)	FLT4 (R1290S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1314540	NM_182925.5(FLT4):c.3862G>C (p.Glu1288Gln)	FLT4 (E1288Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 3340909	NM_182925.5(FLT4):c.3823A>G (p.Ser1275Gly)	FLT4 (S1275G)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 1236979	NM_182925.5(FLT4):c.3808-186C>T	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263780	NM_182925.5(FLT4):c.3808-265T>C	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 263052	NM_182925.5(FLT4):c.3807+34G>C	FLT4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 1279155	NM_182925.5(FLT4):c.3687-292G>A	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247425	NM_182925.5(FLT4):c.3686+79dup	FLT4	Duplication (intron variant)	not provided	GBenign
Select item 3367357	NM_182925.5(FLT4):c.3538G>C (p.Glu1180Gln)	FLT4 (E1180Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1282154	NM_182925.5(FLT4):c.3538-66T>C	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227962	NM_182925.5(FLT4):c.3538-201_3538-200del	FLT4	Deletion (intron variant)	not provided	GBenign
Select item 1273581	NM_182925.5(FLT4):c.3538-217G>A	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268628	NM_182925.5(FLT4):c.3538-232G>A	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252296	NM_182925.5(FLT4):c.3537+319T>C	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3343300	NM_182925.5(FLT4):c.3486C>A (p.Phe1162Leu)	FLT4 (F1162L)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 3373154	NM_182925.5(FLT4):c.3473C>T (p.Ala1158Val)	FLT4 (A1158V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 3366209	NM_182925.5(FLT4):c.3432-13C>A	FLT4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 932061	NM_182925.5(FLT4):c.3410C>T (p.Pro1137Leu)	FLT4 (P1137L)	Single nucleotide variant (missense variant)	not provided +2 more	GLikely pathogenic
Select item 1209909	NM_182925.5(FLT4):c.3391G>C (p.Gly1131Arg)	FLT4 (G1131R)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 1273729	NM_182925.5(FLT4):c.3331+328A>G	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260711	NM_182925.5(FLT4):c.3331+150C>T	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264373	NM_182925.5(FLT4):c.3331+67C>G	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247834	NM_182925.5(FLT4):c.3331+60A>G	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3365881	NM_182925.5(FLT4):c.3296C>T (p.Ser1099Phe)	FLT4 (S1099F)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
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 1309907	NM_182925.5(FLT4):c.3262G>A (p.Asp1088Asn)	FLT4 (D1088N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1803467	NM_182925.5(FLT4):c.3242T>G (p.Met1081Arg)	FLT4 (M1081R)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
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 1265136	NM_182925.5(FLT4):c.3220-63A>G	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257792	NM_182925.5(FLT4):c.3220-95_3220-94insCCGCG	FLT4	Insertion (intron variant)	not provided	GBenign
Select item 1236590	NM_182925.5(FLT4):c.3220-95_3220-94insCG	FLT4	Insertion (intron variant)	not provided	GBenign
Select item 1247517	NM_182925.5(FLT4):c.3220-95A>G	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289040	NM_182925.5(FLT4):c.3220-137T>C	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235762	NM_182925.5(FLT4):c.3220-312G>A	FLT4	Single nucleotide variant (intron variant)	not provided	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 1331243	NM_182925.5(FLT4):c.3208C>T (p.Arg1070Cys)	FLT4 (R1070C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3368423	NM_182925.5(FLT4):c.3205G>C (p.Val1069Leu)	FLT4 (V1069L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 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 1315232	NM_182925.5(FLT4):c.3179G>C (p.Arg1060Pro)	FLT4 (R1060P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1309785	NM_182925.5(FLT4):c.3175G>C (p.Ala1059Pro)	FLT4 (A1059P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1706213	NM_182925.5(FLT4):c.3170G>A (p.Gly1057Asp)	FLT4 (G1057D)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 1712154	NM_182925.5(FLT4):c.3122G>A (p.Arg1041Gln)	FLT4 (R1041Q)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 16260	NM_182925.5(FLT4):c.3122G>C (p.Arg1041Pro)	FLT4 (R1041P)	Single nucleotide variant (missense variant)	not provided	GPathogenic
Select item 692043	NM_182925.5(FLT4):c.3121C>T (p.Arg1041Trp)	FLT4 (R1041W)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1290786	NM_182925.5(FLT4):c.3096+169G>T	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3372546	NM_182925.5(FLT4):c.3037G>T (p.Asp1013Tyr)	FLT4 (D1013Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1297745	NM_182925.5(FLT4):c.3023C>T (p.Pro1008Leu)	FLT4 (P1008L)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1245840	NM_182925.5(FLT4):c.3001+69_3001+70insCCTAGGGTAA	FLT4	Insertion (intron variant)	not provided	GBenign
Select item 263040	NM_182925.5(FLT4):c.2761+44G>A	FLT4	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 2412885	NM_182925.5(FLT4):c.2758C>G (p.Gln920Glu)	FLT4 (Q920E)	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 263039	NM_182925.5(FLT4):c.2670C>G (p.His890Gln)	FLT4 (H890Q)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 1229608	NM_182925.5(FLT4):c.2648-61_2648-60insCTGTGCCTTAGCTAAGCGGCCA	FLT4	Insertion (intron variant)	not provided	GBenign
Select item 1277383	NM_182925.5(FLT4):c.2648-128_2648-127del	FLT4	Microsatellite (intron variant)	not provided	GBenign
Select item 1231940	NM_182925.5(FLT4):c.2647+29C>G	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 16259	NM_182925.5(FLT4):c.2569G>A (p.Gly857Arg)	FLT4 (G857R)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic
Select item 16269	NM_182925.5(FLT4):c.2563G>A (p.Ala855Thr)	FLT4 (A855T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1264896	NM_182925.5(FLT4):c.2543-70C>T	FLT4, LOC126807632	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222591	NM_182925.5(FLT4):c.2543-116C>T	FLT4, LOC126807632	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275998	NM_182925.5(FLT4):c.2543-165C>A	FLT4, LOC126807632	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1698170	NM_182925.5(FLT4):c.2515G>A (p.Glu839Lys)	FLT4, LOC126807632 (E839K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1179458	NM_182925.5(FLT4):c.2407-104A>G	FLT4, LOC126807632	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283473	NM_182925.5(FLT4):c.2300-42AC[11]	FLT4, LOC126807632	Microsatellite (intron variant)	not provided	GBenign
Select item 1224240	NM_182925.5(FLT4):c.2300-42AC[10]	FLT4, LOC126807632	Microsatellite (intron variant)	not provided	GBenign
Select item 1276849	NM_182925.5(FLT4):c.2300-78C>G	FLT4, LOC126807632	Single nucleotide variant (intron variant)	not provided	GBenign
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 1295068	NM_182925.5(FLT4):c.2021-64G>C	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
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 3377919	NM_182925.5(FLT4):c.1775G>A (p.Arg592His)	FLT4 (R592H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1264431	NM_182925.5(FLT4):c.1658-68G>T	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259157	NM_182925.5(FLT4):c.1658-98GAGG[5]	FLT4	Microsatellite (intron variant)	not provided	GBenign
Select item 1283099	NM_182925.5(FLT4):c.1658-248G>A	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227487	NM_182925.5(FLT4):c.1658-274C>G	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275381	NM_182925.5(FLT4):c.1658-277G>A	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179713	NM_182925.5(FLT4):c.1657+206A>G	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260160	NM_182925.5(FLT4):c.1657+113T>C	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
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 1232055	NM_182925.5(FLT4):c.1549-68C>T	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252534	NM_182925.5(FLT4):c.1549-87_1549-85del	FLT4	Microsatellite (intron variant)	not provided	GBenign
Select item 1289242	NM_182925.5(FLT4):c.1549-89_1549-88del	FLT4	Deletion (intron variant)	not provided	GBenign
Select item 1290250	NM_182925.5(FLT4):c.1549-89del	FLT4	Deletion (intron variant)	not provided	GBenign
Select item 1286102	NM_182925.5(FLT4):c.1549-89T>G	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1177684	NM_182925.5(FLT4):c.1549-104del	FLT4	Deletion (intron variant)	not provided	GBenign
Select item 1290906	NM_182925.5(FLT4):c.1549-309A>G	FLT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249850	NM_182925.5(FLT4):c.1549-324G>A	FLT4	Single nucleotide variant (intron variant)	not provided	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

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