"Invitae"[submitter] AND "FLT3"[gene] - ClinVar

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Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 776787	NM_004119.3(FLT3):c.2979G>A (p.Ser993=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 134441	NM_004119.3(FLT3):c.2962G>C (p.Ala988Pro)	FLT3 (A988P)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 134440	NM_004119.3(FLT3):c.2918G>A (p.Arg973Gln)	FLT3 (R973Q)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 134438	NM_004119.3(FLT3):c.2888C>T (p.Ser963Leu)	FLT3 (S963L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 710610	NM_004119.3(FLT3):c.2823G>A (p.Ser941=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 731549	NM_004119.3(FLT3):c.2679G>A (p.Pro893=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 744507	NM_004119.3(FLT3):c.2622T>C (p.Tyr874=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2064171	NM_004119.3(FLT3):c.2554G>A (p.Val852Ile)	FLT3 (V852I)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 725869	NM_004119.3(FLT3):c.2448C>T (p.Asn816=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 727593	NM_004119.3(FLT3):c.2415G>A (p.Lys805=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 737902	NM_004119.3(FLT3):c.2205C>T (p.Ser735=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 735586	NM_004119.3(FLT3):c.2199A>G (p.Pro733=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 735735	NM_004119.3(FLT3):c.2046A>G (p.Thr682=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 738294	NM_004119.3(FLT3):c.1942+8A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 748751	NM_004119.3(FLT3):c.1926C>T (p.Ala642=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 776788	NM_004119.3(FLT3):c.1815T>C (p.Phe605=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 785441	NM_004119.3(FLT3):c.1773C>T (p.Tyr591=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 781984	NM_004119.3(FLT3):c.1597+8A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 741698	NM_004119.3(FLT3):c.1597+7C>T	FLT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 768607	NM_004119.3(FLT3):c.1578G>C (p.Thr526=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1092736	NM_004119.3(FLT3):c.1519A>G (p.Ile507Val)	FLT3 (I507V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 773836	NM_004119.3(FLT3):c.1423A>C (p.Thr475Pro)	FLT3 (T475P)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 748059	NM_004119.3(FLT3):c.1380A>G (p.Pro460=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 769395	NM_004119.3(FLT3):c.1278A>G (p.Gln426=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 134433	NM_004119.3(FLT3):c.1249A>C (p.Ile417Leu)	FLT3 (I417L)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 134452	NM_004119.3(FLT3):c.1073A>T (p.Asp358Val)	FLT3 (D358V)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 759650	NM_004119.3(FLT3):c.1036+8A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 729060	NM_004119.3(FLT3):c.1032C>T (p.Ile344=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 762217	NM_004119.3(FLT3):c.1014A>G (p.Gln338=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 793602	NM_004119.3(FLT3):c.972C>T (p.Asp324=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 720701	NM_004119.3(FLT3):c.743-9A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 795908	NM_004119.3(FLT3):c.742+9A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 728968	NM_004119.3(FLT3):c.728G>A (p.Arg243Lys)	FLT3 (R243K)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 134446	NM_004119.3(FLT3):c.580G>A (p.Val194Met)	FLT3 (V194M)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 735026	NM_004119.3(FLT3):c.540C>T (p.Asp180=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 725922	NM_004119.3(FLT3):c.484+8C>T	FLT3	Single nucleotide variant (intron variant)	FLT3-related condition +1 more	GBenign/Likely benign
Select item 754439	NM_004119.3(FLT3):c.420A>G (p.Glu140=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 753971	NM_004119.3(FLT3):c.369-4G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 744282	NM_004119.3(FLT3):c.347C>G (p.Pro116Arg)	FLT3 (P116R)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 735561	NM_004119.3(FLT3):c.180G>A (p.Pro60=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 741061	NM_004119.3(FLT3):c.166-4G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 744482	NM_004119.3(FLT3):c.166-5C>T	FLT3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 741728	NM_004119.3(FLT3):c.144G>A (p.Gly48=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 787677	NM_004119.3(FLT3):c.96G>C (p.Val32=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 134436	NM_004119.3(FLT3):c.46G>C (p.Val16Leu)	FLT3 (V16L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

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Items: 45