"Ambry Genetics"[submitter] AND "ZDHHC19"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2206867	NM_001039617.2(ZDHHC19):c.922G>T (p.Ala308Ser)	ZDHHC19 (A308S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589107	NM_001039617.2(ZDHHC19):c.853T>C (p.Ser285Pro)	ZDHHC19 (S285P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261608	NM_001039617.2(ZDHHC19):c.724G>C (p.Gly242Arg)	ZDHHC19 (G242R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192691	NM_001039617.2(ZDHHC19):c.721C>A (p.Gln241Lys)	ZDHHC19 (Q241K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192690	NM_001039617.2(ZDHHC19):c.718G>A (p.Asp240Asn)	ZDHHC19 (D240N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296396	NM_001039617.2(ZDHHC19):c.664G>A (p.Ala222Thr)	ZDHHC19 (A222T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337058	NM_001039617.2(ZDHHC19):c.503C>T (p.Ser168Leu)	ZDHHC19 (S168L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316982	NM_001039617.2(ZDHHC19):c.463C>G (p.Arg155Gly)	ZDHHC19 (R155G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192689	NM_001039617.2(ZDHHC19):c.440A>T (p.Asn147Ile)	ZDHHC19 (N147I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389007	NM_001039617.2(ZDHHC19):c.362G>A (p.Arg121His)	ZDHHC19 (R121H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330751	NM_001039617.2(ZDHHC19):c.361C>T (p.Arg121Cys)	ZDHHC19 (R121C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459217	NM_001039617.2(ZDHHC19):c.336A>C (p.Gln112His)	ZDHHC19 (Q112H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192688	NM_001039617.2(ZDHHC19):c.328C>T (p.Arg110Cys)	ZDHHC19 (R110C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192687	NM_001039617.2(ZDHHC19):c.299A>G (p.His100Arg)	ZDHHC19 (H100R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477097	NM_001039617.2(ZDHHC19):c.229G>A (p.Val77Ile)	ZDHHC19 (V77I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2470379	NM_001039617.2(ZDHHC19):c.215C>T (p.Thr72Ile)	ZDHHC19 (T72I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192686	NM_001039617.2(ZDHHC19):c.196G>A (p.Gly66Ser)	ZDHHC19 (G66S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2565863	NM_001039617.2(ZDHHC19):c.143T>G (p.Phe48Cys)	ZDHHC19 (F48C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545695	NM_001039617.2(ZDHHC19):c.128G>A (p.Gly43Asp)	ZDHHC19 (G43D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488436	NM_001039617.2(ZDHHC19):c.118T>C (p.Phe40Leu)	ZDHHC19 (F40L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471334	NM_001039617.2(ZDHHC19):c.115G>C (p.Val39Leu)	ZDHHC19 (V39L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276802	NM_001039617.2(ZDHHC19):c.61C>T (p.Pro21Ser)	ZDHHC19 (P21S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541035	NM_001039617.2(ZDHHC19):c.43C>T (p.His15Tyr)	ZDHHC19 (H15Y)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2558560	NM_001039617.2(ZDHHC19):c.26C>T (p.Pro9Leu)	ZDHHC19 (P9L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24