"Ambry Genetics"[submitter] AND "FLT1"[gene] - ClinVar

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Items: 56

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3095725	NM_002019.4(FLT1):c.3984C>A (p.Asn1328Lys)	FLT1 (N1328K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279253	NM_002019.4(FLT1):c.3956C>T (p.Ala1319Val)	FLT1 (A1319V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605373	NM_002019.4(FLT1):c.3926A>G (p.Tyr1309Cys)	FLT1 (Y1309C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095724	NM_002019.4(FLT1):c.3805C>T (p.Leu1269Phe)	FLT1 (L1269F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095723	NM_002019.4(FLT1):c.3800C>G (p.Ala1267Gly)	FLT1 (A1267G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095722	NM_002019.4(FLT1):c.3770G>A (p.Arg1257His)	FLT1 (R1257H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240195	NM_002019.4(FLT1):c.3599C>T (p.Ala1200Val)	FLT1 (A1200V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317629	NM_002019.4(FLT1):c.3563C>A (p.Ala1188Asp)	FLT1 (A1188D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095721	NM_002019.4(FLT1):c.3493G>A (p.Asp1165Asn)	FLT1 (D1165N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095720	NM_002019.4(FLT1):c.3471G>C (p.Leu1157Phe)	FLT1 (L1157F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095719	NM_002019.4(FLT1):c.3307G>C (p.Val1103Leu)	FLT1 (V1103L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095718	NM_002019.4(FLT1):c.3289G>A (p.Gly1097Arg)	FLT1 (G1097R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095717	NM_002019.4(FLT1):c.3287G>A (p.Gly1096Asp)	FLT1 (G1096D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279255	NM_002019.4(FLT1):c.3220A>C (p.Lys1074Gln)	FLT1 (K1074Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095716	NM_002019.4(FLT1):c.3197T>C (p.Met1066Thr)	FLT1 (M1066T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229481	NM_002019.4(FLT1):c.3096G>C (p.Glu1032Asp)	FLT1 (E1032D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554668	NM_002019.4(FLT1):c.3055A>G (p.Ile1019Val)	FLT1 (I1019V)	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 2488843	NM_002019.4(FLT1):c.2834T>C (p.Met945Thr)	FLT1, LOC126861720 (M945T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369803	NM_002019.4(FLT1):c.2659C>A (p.His887Asn)	FLT1 (H887N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305257	NM_002019.4(FLT1):c.2596G>A (p.Gly866Arg)	FLT1 (G866R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095715	NM_002019.4(FLT1):c.2437C>A (p.Leu813Ile)	FLT1 (L813I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095714	NM_002019.4(FLT1):c.2152A>T (p.Ile718Phe)	FLT1 (I718F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519959	NM_002019.4(FLT1):c.2065G>A (p.Glu689Lys)	FLT1 (E689K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261537	NM_002019.4(FLT1):c.2062C>G (p.Pro688Ala)	FLT1 (P688A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335441	NM_002019.4(FLT1):c.2054A>G (p.Asn685Ser)	FLT1 (N685S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611739	NM_002019.4(FLT1):c.1960A>T (p.Thr654Ser)	FLT1 (T654S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095713	NM_002019.4(FLT1):c.1916G>C (p.Arg639Thr)	FLT1 (R639T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301929	NM_002019.4(FLT1):c.1871T>C (p.Met624Thr)	FLT1 (M624T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515731	NM_002019.4(FLT1):c.1800G>T (p.Met600Ile)	FLT1 (M600I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596209	NM_002019.4(FLT1):c.1781C>T (p.Thr594Ile)	FLT1 (T594I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363994	NM_002019.4(FLT1):c.1693A>G (p.Lys565Glu)	FLT1 (K565E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255424	NM_002019.4(FLT1):c.1582A>G (p.Arg528Gly)	FLT1 (R528G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095712	NM_002019.4(FLT1):c.1516A>G (p.Thr506Ala)	FLT1 (T506A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279256	NM_002019.4(FLT1):c.1505T>C (p.Ile502Thr)	FLT1 (I502T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095711	NM_002019.4(FLT1):c.1502G>A (p.Arg501Lys)	FLT1 (R501K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604283	NM_002019.4(FLT1):c.1484A>G (p.Asp495Gly)	FLT1 (D495G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327439	NM_002019.4(FLT1):c.1300G>A (p.Ala434Thr)	FLT1 (A434T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529871	NM_002019.4(FLT1):c.1261A>T (p.Thr421Ser)	FLT1 (T421S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614465	NM_002019.4(FLT1):c.1214T>C (p.Ile405Thr)	FLT1 (I405T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472877	NM_002019.4(FLT1):c.1141G>C (p.Ala381Pro)	FLT1 (A381P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279254	NM_002019.4(FLT1):c.1034A>G (p.Glu345Gly)	FLT1, LOC130009458 (E345G)	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 2466956	NM_002019.4(FLT1):c.871A>G (p.Ile291Val)	FLT1 (I291V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2549216	NM_002019.4(FLT1):c.863A>T (p.His288Leu)	FLT1 (H288L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385100	NM_002019.4(FLT1):c.855C>G (p.Ser285Arg)	FLT1 (S285R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3095728	NM_002019.4(FLT1):c.839G>A (p.Arg280Gln)	FLT1 (R280Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2298828	NM_002019.4(FLT1):c.742C>T (p.Leu248Phe)	FLT1 (L248F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095727	NM_002019.4(FLT1):c.665C>T (p.Thr222Ile)	FLT1 (T222I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251774	NM_002019.4(FLT1):c.631G>A (p.Val211Ile)	FLT1 (V211I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2562566	NM_002019.4(FLT1):c.547C>T (p.Arg183Cys)	FLT1 (R183C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095726	NM_002019.4(FLT1):c.493A>G (p.Ile165Val)	FLT1 (I165V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519090	NM_002019.4(FLT1):c.476G>A (p.Arg159Gln)	FLT1 (R159Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279257	NM_002019.4(FLT1):c.457G>A (p.Glu153Lys)	FLT1 (E153K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559623	NM_002019.4(FLT1):c.209A>G (p.Glu70Gly)	FLT1 (E70G)	Single nucleotide variant (missense variant)	not specified	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

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Items: 56