Related gene-specific medical variations for Gene (Select 2321) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2488843	NM_002019.4(FLT1):c.2834T>C (p.Met945Thr)	FLT1, LOC126861720 (M945T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2431148	NM_002019.4(FLT1):c.64+22G>T	FLT1, LOC130009460	Single nucleotide variant (intron variant)	Squamous cell carcinoma	GUncertain significance
Select item 2431119	NM_002019.4(FLT1):c.3174+225T>G	FLT1, LOC124849303	Single nucleotide variant (intron variant)	Lung adenocarcinoma	GUncertain significance
Select item 2296986	NM_002019.4(FLT1):c.4G>A (p.Val2Ile)	FLT1, LOC130009460 (V2I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243262	NM_002019.4(FLT1):c.2962G>A (p.Gly988Ser)	FLT1, LOC126861720 (G988S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229518	NM_002019.4(FLT1):c.1022A>G (p.Gln341Arg)	FLT1, LOC130009458 (Q341R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 778082	NM_002019.4(FLT1):c.2812A>G (p.Met938Val)	FLT1, LOC126861720 (M938V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 730494	NM_002019.4(FLT1):c.1095G>A (p.Pro365=)	FLT1, LOC130009458	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 727121	NM_002019.4(FLT1):c.16G>A (p.Asp6Asn)	FLT1, LOC130009460 (D6N)	Single nucleotide variant (missense variant)	not provided	GBenign
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 162071	NM_002019.4(FLT1):c.3287-16A>C	FLT1	Single nucleotide variant (intron variant)	Carcinoma of colon	Gnot provided