"Ambry Genetics"[submitter] AND "DUSP29"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3086325	NM_001003892.3(DUSP29):c.629A>G (p.Gln210Arg)	DUSP29 (Q210R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086324	NM_001003892.3(DUSP29):c.614G>A (p.Arg205Gln)	DUSP29 (R205Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274076	NM_001003892.3(DUSP29):c.554C>T (p.Pro185Leu)	DUSP29 (P185L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086323	NM_001003892.3(DUSP29):c.500A>T (p.Asp167Val)	DUSP29 (D167V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467672	NM_001003892.3(DUSP29):c.497A>G (p.Lys166Arg)	DUSP29 (K166R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3086322	NM_001003892.3(DUSP29):c.452G>A (p.Arg151His)	DUSP29 (R151H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475268	NM_001003892.3(DUSP29):c.449G>T (p.Gly150Val)	DUSP29 (G150V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086320	NM_001003892.3(DUSP29):c.427A>G (p.Ile143Val)	DUSP29 (I143V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274075	NM_001003892.3(DUSP29):c.380C>G (p.Pro127Arg)	DUSP29 (P127R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086319	NM_001003892.3(DUSP29):c.365G>C (p.Ser122Thr)	DUSP29, LOC130004128 (S122T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086318	NM_001003892.3(DUSP29):c.353C>T (p.Thr118Ile)	DUSP29, LOC130004128 (T118I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086317	NM_001003892.3(DUSP29):c.346C>G (p.Leu116Val)	DUSP29, LOC130004128 (L116V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2557934	NM_001003892.3(DUSP29):c.295G>A (p.Asp99Asn)	DUSP29, LOC130004128 (D99N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517730	NM_001003892.3(DUSP29):c.293C>T (p.Pro98Leu)	DUSP29, LOC130004128 (P98L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086316	NM_001003892.3(DUSP29):c.250G>A (p.Val84Met)	DUSP29, LOC130004128 (V84M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086315	NM_001003892.3(DUSP29):c.162C>G (p.His54Gln)	DUSP29 (H54Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537989	NM_001003892.3(DUSP29):c.162C>A (p.His54Gln)	DUSP29 (H54Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591423	NM_001003892.3(DUSP29):c.127C>T (p.Arg43Trp)	DUSP29 (R43W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558438	NM_001003892.3(DUSP29):c.113C>G (p.Ala38Gly)	DUSP29 (A38G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274077	NM_001003892.3(DUSP29):c.98A>G (p.Tyr33Cys)	DUSP29 (Y33C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274074	NM_001003892.3(DUSP29):c.26G>A (p.Ser9Asn)	DUSP29 (S9N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 21