"ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories - 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 1330670	NM_182925.5(FLT4):c.4006G>A (p.Glu1336Lys)	FLT4 (E1336K)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 263055	NM_182925.5(FLT4):c.3962G>A (p.Arg1321Gln)	FLT4 (R1321Q)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 263054	NM_182925.5(FLT4):c.3959G>A (p.Arg1320Gln)	FLT4 (R1320Q)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 263053	NM_182925.5(FLT4):c.3908G>C (p.Gly1303Ala)	FLT4 (G1303A)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 701829	NM_182925.5(FLT4):c.3681C>T (p.Ala1227=)	FLT4	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 702108	NM_182925.5(FLT4):c.3460G>A (p.Gly1154Arg)	FLT4 (G1154R)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 994302	NM_182925.5(FLT4):c.3436C>G (p.Arg1146Gly)	FLT4 (R1146G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 263043	NM_182925.5(FLT4):c.3147C>T (p.Asp1049=)	FLT4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 811871	NM_182925.5(FLT4):c.3108A>T (p.Arg1036Ser)	FLT4 (R1036S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 263042	NM_182925.5(FLT4):c.3002-18C>A	FLT4	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 16264	NM_182925.5(FLT4):c.2860C>T (p.Pro954Ser)	FLT4 (P954S)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 811370	NM_182925.5(FLT4):c.2648-8C>T	FLT4	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 811632	NM_182925.5(FLT4):c.2407-18C>T	FLT4, LOC126807632	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 1331051	NM_182925.5(FLT4):c.2002A>G (p.Lys668Glu)	FLT4 (K668E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 263032	NM_182925.5(FLT4):c.1921C>T (p.Pro641Ser)	FLT4 (P641S)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 993824	NM_182925.5(FLT4):c.1581C>T (p.Asn527=)	FLT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 263029	NM_182925.5(FLT4):c.1580A>G (p.Asn527Ser)	FLT4 (N527S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 995590	NM_182925.5(FLT4):c.1452A>G (p.Pro484=)	FLT4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1330716	NM_182925.5(FLT4):c.1133G>A (p.Arg378His)	FLT4 (R378H)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 263067	NM_182925.5(FLT4):c.633A>G (p.Gly211=)	FLT4	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 1330711	NM_182925.5(FLT4):c.504G>A (p.Thr168=)	FLT4	Single nucleotide variant (synonymous variant)	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