ClinVar (all) for Orgtrack (Select 505308) - ClinVar

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Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 204359	NM_002019.4(FLT1):c.2439_2466del (p.Tyr815fs)	FLT1 (Y815fs)	Deletion (frameshift variant)	Carcinoma of colon	GUncertain significance
Select item 204358	NM_182925.5(FLT4):c.3002-9A>C	FLT4	Single nucleotide variant (intron variant)	Carcinoma of colon	GUncertain significance
Select item 204357	NM_182925.5(FLT4):c.3056del (p.Phe1019fs)	FLT4 (F1019fs)	Deletion (frameshift variant)	Carcinoma of colon	GUncertain significance
Select item 204356	NM_182925.5(FLT4):c.3064del (p.Ala1022fs)	FLT4 (A1022fs)	Deletion (frameshift variant)	Carcinoma of colon	GUncertain significance
Select item 204355	NM_182925.5(FLT4):c.3065C>T (p.Ala1022Val)	FLT4 (A1022V)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204354	NM_182925.5(FLT4):c.3072del (p.Met1025fs)	FLT4 (M1025fs)	Deletion (frameshift variant)	Carcinoma of colon	GUncertain significance
Select item 204353	NM_182925.5(FLT4):c.3076del (p.Glu1026fs)	FLT4 (E1026fs)	Deletion (frameshift variant)	Carcinoma of colon	GUncertain significance
Select item 204352	NM_182925.5(FLT4):c.2647+31del	FLT4	Deletion (intron variant)	Carcinoma of colon	GUncertain significance
Select item 204351	NM_182925.5(FLT4):c.2407-7C>T	FLT4, LOC126807632	Single nucleotide variant (intron variant)	Carcinoma of colon	GUncertain significance
Select item 204350	NM_182925.5(FLT4):c.2407-6C>G	FLT4, LOC126807632	Single nucleotide variant (intron variant)	Carcinoma of colon	GUncertain significance
Select item 204349	NM_182925.5(FLT4):c.2414A>C (p.His805Pro)	FLT4, LOC126807632 (H805P)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204348	NM_182925.5(FLT4):c.2433C>A (p.Gly811=)	FLT4, LOC126807632	Single nucleotide variant (synonymous variant)	Carcinoma of colon	GUncertain significance
Select item 204347	NM_182925.5(FLT4):c.2470C>A (p.Leu824Met)	FLT4, LOC126807632 (L824M)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204346	NM_182925.5(FLT4):c.2496C>G (p.Ser832=)	FLT4, LOC126807632	Single nucleotide variant (synonymous variant)	Carcinoma of colon	GUncertain significance
Select item 204345	NM_182925.5(FLT4):c.2498A>C (p.Tyr833Ser)	FLT4, LOC126807632 (Y833S)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204344	NM_182925.5(FLT4):c.2502T>A (p.Asp834Glu)	FLT4, LOC126807632 (D834E)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204343	NM_182925.5(FLT4):c.2507G>A (p.Ser836Asn)	FLT4, LOC126807632 (S836N)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204342	NM_182925.5(FLT4):c.2519del (p.Phe840fs)	FLT4, LOC126807632 (F840fs)	Deletion (frameshift variant)	Carcinoma of colon	GUncertain significance
Select item 204341	NM_182925.5(FLT4):c.2542+12A>G	FLT4, LOC126807632	Single nucleotide variant (intron variant)	Carcinoma of colon	GUncertain significance
Select item 204340	NM_182925.5(FLT4):c.2542+18del	FLT4, LOC126807632	Deletion (intron variant)	Carcinoma of colon	GUncertain significance
Select item 204339	NM_182925.5(FLT4):c.2542+20del	FLT4, LOC126807632	Deletion (intron variant)	Carcinoma of colon	GUncertain significance
Select item 204338	NM_002253.4(KDR):c.3487C>T (p.Leu1163Phe)	KDR (L1163F)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204337	NM_002253.4(KDR):c.3465G>A (p.Glu1155=)	KDR	Single nucleotide variant (synonymous variant)	Carcinoma of colon	GUncertain significance
Select item 204336	NM_002253.4(KDR):c.3441C>G (p.Pro1147=)	KDR	Single nucleotide variant (synonymous variant)	Carcinoma of colon	GUncertain significance
Select item 204335	NM_002253.4(KDR):c.3405-4C>T	KDR	Single nucleotide variant (intron variant)	Carcinoma of colon	GUncertain significance
Select item 204334	NM_002253.4(KDR):c.2598A>C (p.Ala866=)	KDR	Single nucleotide variant (synonymous variant)	Carcinoma of colon	GUncertain significance
Select item 204333	NM_002253.4(KDR):c.2544G>T (p.Val848=)	KDR	Single nucleotide variant (synonymous variant)	Carcinoma of colon	GUncertain significance
Select item 204332	NM_002253.4(KDR):c.2510-27del	KDR	Deletion (intron variant)	Carcinoma of colon	GUncertain significance
Select item 204331	NM_002253.4(KDR):c.2509+20T>A	KDR	Single nucleotide variant (intron variant)	Carcinoma of colon	GUncertain significance
Select item 204330	NM_002253.4(KDR):c.2380G>A (p.Gly794Arg)	KDR (G794R)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204329	NM_002253.4(KDR):c.2721G>C (p.Lys907Asn)	KDR (K907N)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204328	NM_002253.4(KDR):c.2705T>A (p.Leu902Gln)	KDR (L902Q)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204327	NM_002253.4(KDR):c.2676T>A (p.Ile892=)	KDR	Single nucleotide variant (synonymous variant)	Carcinoma of colon	GUncertain significance
Select item 204326	NM_002253.4(KDR):c.2656C>A (p.Leu886Ile)	KDR (L886I)	Single nucleotide variant (missense variant)	Carcinoma of colon	GUncertain significance
Select item 204325	NM_002253.4(KDR):c.2615-23C>T	KDR	Single nucleotide variant (intron variant)	Carcinoma of colon	GUncertain significance
Select item 183436	NM_002019.4(FLT1):c.3329G>C (p.Cys1110Ser)	FLT1 (C1110S)	Single nucleotide variant (missense variant)	Carcinoma of colon	Gnot provided
Select item 162079	NM_002019.4(FLT1):c.2871A>T (p.Leu957=)	FLT1, LOC126861720	Single nucleotide variant (synonymous variant)	Carcinoma of colon	Gnot provided
Select item 162078	NM_002019.4(FLT1):c.2901G>A (p.Ala967=)	FLT1, LOC126861720	Single nucleotide variant (synonymous variant)	Carcinoma of colon	Gnot provided
Select item 162077	NM_002019.4(FLT1):c.2654_2655insA (p.Gly886fs)	FLT1 (G886fs)	Insertion (frameshift variant)	Carcinoma of colon	Gnot provided
Select item 162076	NM_002019.4(FLT1):c.2708-39G>C	FLT1	Single nucleotide variant (intron variant)	Carcinoma of colon	Gnot provided
Select item 162075	NM_002019.4(FLT1):c.2708-29A>C	FLT1	Single nucleotide variant (intron variant)	Carcinoma of colon	Gnot provided
Select item 162074	NM_002019.4(FLT1):c.3042_3043insA (p.Ser1015fs)	FLT1, LOC126861720 (S1015fs)	Insertion (frameshift variant)	Carcinoma of colon	Gnot provided
Select item 162073	NM_002019.4(FLT1):c.3175-69A>T	FLT1	Single nucleotide variant (intron variant)	Carcinoma of colon	Gnot provided
Select item 162072	NM_002019.4(FLT1):c.3204T>C (p.Pro1068=)	FLT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 162071	NM_002019.4(FLT1):c.3287-16A>C	FLT1	Single nucleotide variant (intron variant)	Carcinoma of colon	Gnot provided

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Items: 45