"Ambry Genetics"[submitter] AND "DUSP5"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2481030	NM_004419.4(DUSP5):c.88C>T (p.Pro30Ser)	DUSP5, LOC130004716 (P30S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590716	NM_004419.4(DUSP5):c.112A>T (p.Asn38Tyr)	DUSP5, LOC130004716 (N38Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531576	NM_004419.4(DUSP5):c.139C>T (p.Leu47Phe)	DUSP5 (L47F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086339	NM_004419.4(DUSP5):c.140T>C (p.Leu47Pro)	DUSP5 (L47P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086340	NM_004419.4(DUSP5):c.167G>C (p.Arg56Pro)	DUSP5 (R56P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261662	NM_004419.4(DUSP5):c.182C>G (p.Ser61Trp)	DUSP5 (S61W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274087	NM_004419.4(DUSP5):c.191A>G (p.Tyr64Cys)	DUSP5 (Y64C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086341	NM_004419.4(DUSP5):c.204C>A (p.Asp68Glu)	DUSP5 (D68E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210421	NM_004419.4(DUSP5):c.233A>T (p.Glu78Val)	DUSP5 (E78V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545352	NM_004419.4(DUSP5):c.280C>T (p.Arg94Cys)	DUSP5, LOC130004717 (R94C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086342	NM_004419.4(DUSP5):c.388G>C (p.Glu130Gln)	DUSP5 (E130Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528726	NM_004419.4(DUSP5):c.427G>A (p.Val143Ile)	DUSP5 (V143I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274088	NM_004419.4(DUSP5):c.491C>G (p.Pro164Arg)	DUSP5 (P164R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526965	NM_004419.4(DUSP5):c.591C>G (p.Cys197Trp)	DUSP5 (C197W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222426	NM_004419.4(DUSP5):c.817A>C (p.Ile273Leu)	DUSP5 (I273L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086343	NM_004419.4(DUSP5):c.854G>A (p.Arg285His)	DUSP5 (R285H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1335047	NM_004419.4(DUSP5):c.871G>A (p.Asp291Asn)	DUSP5 (D291N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2553973	NM_004419.4(DUSP5):c.1047G>A (p.Met349Ile)	DUSP5 (M349I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510853	NM_004419.4(DUSP5):c.1076C>T (p.Ser359Leu)	DUSP5 (S359L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410283	NM_004419.4(DUSP5):c.1088C>T (p.Pro363Leu)	DUSP5 (P363L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513591	NM_004419.4(DUSP5):c.1103C>T (p.Ser368Leu)	DUSP5 (S368L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 21