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

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2352473	NM_003377.5(VEGFB):c.8C>T (p.Pro3Leu)	VEGFB (P3L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270995	NM_003377.5(VEGFB):c.28C>G (p.Leu10Val)	LOC130005920, VEGFB (L10V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593651	NM_003377.5(VEGFB):c.31G>A (p.Ala11Thr)	LOC130005920, VEGFB (A11T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3331998	NM_003377.5(VEGFB):c.53C>G (p.Pro18Arg)	LOC130005920, VEGFB (P18R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596885	NM_003377.5(VEGFB):c.68T>C (p.Val23Ala)	VEGFB (V23A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539151	NM_003377.5(VEGFB):c.86C>G (p.Pro29Arg)	VEGFB (P29R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590225	NM_003377.5(VEGFB):c.131G>A (p.Arg44His)	VEGFB (R44H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615410	NM_003377.5(VEGFB):c.133G>A (p.Ala45Thr)	VEGFB (A45T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210662	NM_003377.5(VEGFB):c.149G>A (p.Arg50Gln)	VEGFB (R50Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188437	NM_003377.5(VEGFB):c.153G>C (p.Glu51Asp)	VEGFB (E51D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188438	NM_003377.5(VEGFB):c.221C>G (p.Thr74Ser)	VEGFB (T74S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188439	NM_003377.5(VEGFB):c.292C>T (p.Arg98Trp)	VEGFB (R98W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292422	NM_003377.5(VEGFB):c.293G>A (p.Arg98Gln)	VEGFB (R98Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188440	NM_003377.5(VEGFB):c.313C>T (p.Arg105Trp)	VEGFB (R105W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257030	NM_003377.5(VEGFB):c.349G>A (p.Glu117Lys)	VEGFB (E117K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470144	NM_003377.5(VEGFB):c.365G>A (p.Cys122Tyr)	VEGFB (C122Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188441	NM_003377.5(VEGFB):c.402G>T (p.Lys134Asn)	VEGFB (K134N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188442	NM_003377.5(VEGFB):c.452C>T (p.Pro151Leu)	VEGFB (P151L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364447	NM_003377.5(VEGFB):c.497C>A (p.Thr166Asn)	VEGFB (T166N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262894	NM_003377.5(VEGFB):c.502C>T (p.Pro168Ser)	VEGFB (P168S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231759	NM_003377.5(VEGFB):c.520C>T (p.Pro174Ser)	VEGFB (P174S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534730	NM_003377.5(VEGFB):c.544A>G (p.Thr182Ala)	VEGFB (T182A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2534731	NM_003377.5(VEGFB):c.547A>G (p.Thr183Ala)	VEGFB (H149R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2346029	NM_003377.5(VEGFB):c.553G>A (p.Ala185Thr)	VEGFB (R151H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534732	NM_003377.5(VEGFB):c.608C>T (p.Ala203Val)	VEGFB (A203V)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance

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Items: 25