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

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 134442	NM_004119.3(FLT3):c.2971G>A (p.Glu991Lys)	FLT3 (E991K)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
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 134439	NM_004119.3(FLT3):c.2957C>T (p.Pro986Leu)	FLT3 (P986L)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
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 134437	NM_004119.3(FLT3):c.2858C>T (p.Ala953Val)	FLT3 (A953V)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134435	NM_004119.3(FLT3):c.2050T>C (p.Ser684Pro)	FLT3 (S684P)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134434	NM_004119.3(FLT3):c.1669G>A (p.Val557Ile)	FLT3 (V557I)	Single nucleotide variant (missense 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 134453	NM_004119.3(FLT3):c.1181A>G (p.Gln394Arg)	FLT3 (Q394R)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
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 134451	NM_004119.3(FLT3):c.970G>A (p.Asp324Asn)	FLT3 (D324N)	Single nucleotide variant (missense variant +1 more)	FLT3-related disorder +1 more	GLikely benign
Select item 134450	NM_004119.3(FLT3):c.844G>A (p.Gly282Arg)	FLT3 (G282R)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134448	NM_004119.3(FLT3):c.833A>C (p.Asn278Thr)	FLT3 (N278T)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134449	NM_004119.3(FLT3):c.784C>T (p.Leu262Phe)	FLT3 (L262F)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134447	NM_004119.3(FLT3):c.680C>T (p.Thr227Met)	FLT3 (T227M)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 134445	NM_004119.3(FLT3):c.605A>G (p.Gln202Arg)	FLT3 (Q202R)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
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 134444	NM_004119.3(FLT3):c.452A>G (p.Asn151Ser)	FLT3 (N151S)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134443	NM_004119.3(FLT3):c.190G>A (p.Gly64Arg)	FLT3 (G64R)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
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

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 21