"Ambry Genetics"[submitter] AND "ZDHHC13"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2390394	NM_019028.3(ZDHHC13):c.8G>C (p.Gly3Ala)	ZDHHC13, LOC130005421 (G3A)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2472222	NM_019028.3(ZDHHC13):c.62G>C (p.Gly21Ala)	ZDHHC13 (G21A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2205847	NM_019028.3(ZDHHC13):c.71G>A (p.Arg24Gln)	ZDHHC13 (R24Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2604295	NM_019028.3(ZDHHC13):c.352A>T (p.Thr118Ser)	ZDHHC13 (T118S)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2546569	NM_019028.3(ZDHHC13):c.413A>G (p.His138Arg)	ZDHHC13 (H138R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2219131	NM_019028.3(ZDHHC13):c.490A>G (p.Ile164Val)	ZDHHC13 (I164V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2319014	NM_019028.3(ZDHHC13):c.495A>G (p.Ile165Met)	ZDHHC13 (I165M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2408322	NM_019028.3(ZDHHC13):c.541A>G (p.Asn181Asp)	ZDHHC13 (N181D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2312131	NM_019028.3(ZDHHC13):c.574A>G (p.Lys192Glu)	ZDHHC13 (K192E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2337543	NM_019028.3(ZDHHC13):c.781A>C (p.Lys261Gln)	ZDHHC13 (K261Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2536104	NM_019028.3(ZDHHC13):c.804G>A (p.Met268Ile)	ZDHHC13 (M268I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2387702	NM_019028.3(ZDHHC13):c.893T>C (p.Leu298Pro)	ZDHHC13 (L168P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2375700	NM_019028.3(ZDHHC13):c.1135A>G (p.Ser379Gly)	ZDHHC13 (S379G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2349281	NM_019028.3(ZDHHC13):c.1522A>G (p.Thr508Ala)	ZDHHC13 (T508A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2489030	NM_019028.3(ZDHHC13):c.1645G>C (p.Gly549Arg)	LOC110121487, ZDHHC13 (G549R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2231945	NM_019028.3(ZDHHC13):c.1651A>T (p.Thr551Ser)	ZDHHC13, LOC110121487 (T421S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2542750	NM_019028.3(ZDHHC13):c.1784T>C (p.Leu595Ser)	ZDHHC13 (L465S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2524711	NM_019028.3(ZDHHC13):c.1859G>C (p.Arg620Pro)	ZDHHC13 (R620P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance