ClinVar for Gene (Select 64429) - ClinVar

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Links from Gene

Items: 63

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3334275	NM_022494.3(ZDHHC6):c.1050G>C (p.Gln350His)	ZDHHC6 (Q242H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334274	NM_022494.3(ZDHHC6):c.451G>A (p.Ala151Thr)	ZDHHC6 (A147T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3334272	NM_022494.3(ZDHHC6):c.154A>G (p.Thr52Ala)	ZDHHC6 (T52A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3334271	NM_022494.3(ZDHHC6):c.754T>C (p.Tyr252His)	ZDHHC6 (Y144H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262947	NM_203379.2(ACSL5):c.1678A>C (p.Asn560His)	ACSL5, ZDHHC6 (N616H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262924	NM_203379.2(ACSL5):c.1723G>A (p.Gly575Arg)	ACSL5, ZDHHC6 (G631R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262898	NM_203379.2(ACSL5):c.2003A>G (p.Lys668Arg)	ACSL5, ZDHHC6 (K700R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192763	NM_022494.3(ZDHHC6):c.518G>A (p.Arg173Gln)	ZDHHC6 (R65Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192762	NM_022494.3(ZDHHC6):c.493A>G (p.Thr165Ala)	ZDHHC6 (T57A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192761	NM_022494.3(ZDHHC6):c.331C>A (p.Arg111Ser)	ZDHHC6 (H37Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3192757	NM_022494.3(ZDHHC6):c.209A>C (p.Tyr70Ser)	ZDHHC6 (Y70S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140065	NM_203379.2(ACSL5):c.1972A>C (p.Thr658Pro)	ACSL5, ZDHHC6 (T658P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140049	NM_203379.2(ACSL5):c.1735C>T (p.Arg579Trp)	ACSL5, ZDHHC6 (R635W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140043	NM_203379.2(ACSL5):c.1673T>C (p.Ile558Thr)	ACSL5, ZDHHC6 (I614T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3063164	GRCh37/hg19 10q23.33-26.3(chr10:95078198-135427143)x3	ABCC2, ABLIM1 +293 more	Copy number gain	not specified	GPathogenic
Select item 3063162	GRCh37/hg19 10q25.1-26.13(chr10:107129993-123817654)x3	ABLIM1, ACSL5 +70 more	Copy number gain	not specified	GLikely pathogenic
Select item 2684622	GRCh37/hg19 10q25.2(chr10:113694296-114349917)x3	ACSL5, GPAM +3 more	Copy number gain	not provided	GUncertain significance
Select item 2684621	GRCh37/hg19 10q25.1-26.3(chr10:111447991-133435388)x3	ABLIM1, ABRAXAS2 +117 more	Copy number gain	not provided	GPathogenic
Select item 2671974	GRCh37/hg19 10q25.1-26.3(chr10:111378692-135427143)x3	ABLIM1, ABRAXAS2 +145 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	AGAP5, CRTAC1 +682 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574686	GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	ABRAXAS2, CHCHD1 +673 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 2557662	NM_022494.3(ZDHHC6):c.433A>C (p.Thr145Pro)	ZDHHC6 (T141P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2555306	NM_022494.3(ZDHHC6):c.28T>C (p.Phe10Leu)	ZDHHC6 (F10L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2540219	NM_022494.3(ZDHHC6):c.17C>T (p.Ser6Leu)	ZDHHC6 (S6L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2535371	NM_022494.3(ZDHHC6):c.1190C>A (p.Pro397His)	ZDHHC6 (P397H +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2529585	NM_203379.2(ACSL5):c.1814C>T (p.Ser605Phe)	ACSL5, ZDHHC6 (S661F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518897	NM_022494.3(ZDHHC6):c.1160G>C (p.Trp387Ser)	ZDHHC6 (W279S +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2508834	NM_022494.3(ZDHHC6):c.137A>G (p.Tyr46Cys)	ZDHHC6 (Y46C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2461113	NM_022494.3(ZDHHC6):c.547A>G (p.Ile183Val)	ZDHHC6 (I179V +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2396424	NM_203379.2(ACSL5):c.1729A>C (p.Ser577Arg)	ACSL5, ZDHHC6 (S577R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336692	NM_203379.2(ACSL5):c.1784C>T (p.Ser595Leu)	ACSL5, ZDHHC6 (S595L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333754	NM_022494.3(ZDHHC6):c.1220A>G (p.Glu407Gly)	ZDHHC6 (E353G +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2314161	NM_022494.3(ZDHHC6):c.712A>G (p.Ile238Val)	ZDHHC6 (I134V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282533	NM_022494.3(ZDHHC6):c.428C>T (p.Ser143Leu)	ZDHHC6 (S143L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2260274	NM_022494.3(ZDHHC6):c.221A>G (p.Asn74Ser)	ZDHHC6 (N74S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2233770	NM_203379.2(ACSL5):c.1613T>C (p.Ile538Thr)	ACSL5, ZDHHC6 (I538T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218935	NM_022494.3(ZDHHC6):c.166G>T (p.Val56Leu)	ZDHHC6 (V56L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 1527605	GRCh37/hg19 10q25.1-26.3(chr10:108455687-135427143)	ABLIM1, ABRAXAS2 +146 more	Copy number gain	not specified	GPathogenic
Select item 1527599	GRCh37/hg19 10q24.32-25.3(chr10:104030479-115410590)	C10orf95, CALHM1 +57 more	Copy number loss	not specified	GPathogenic
Select item 1340153	GRCh37/hg19 10q25.1-25.3(chr10:107092654-117852548)x1	ABLIM1, ACSL5 +32 more	Copy number loss	not provided	GUncertain significance
Select item 779123	NM_022494.3(ZDHHC6):c.606A>G (p.Ala202=)	ZDHHC6	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 778473	NM_022494.3(ZDHHC6):c.726T>C (p.Ile242=)	ZDHHC6	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 711915	NM_022494.3(ZDHHC6):c.634T>C (p.Leu212=)	ZDHHC6	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 625657	GRCh37/hg19 10q25.1-26.3(chr10:110022170-135439095)	ABLIM1, ABRAXAS2 +146 more	Copy number gain	not provided	GPathogenic
Select item 563802	GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3	ABCC2, ABLIM1 +298 more	Copy number gain	not provided	GPathogenic
Select item 563801	GRCh37/hg19 10q24.33-26.3(chr10:105613040-135427143)x3	ABLIM1, ABRAXAS2 +157 more	Copy number gain	not provided	GPathogenic
Select item 563703	GRCh37/hg19 10q25.2(chr10:114195933-114306003)x1	VTI1A, ZDHHC6	Copy number loss	not provided	GLikely benign
Select item 523165	GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1	COX15, CPEB3 +569 more	Copy number loss	Poly (ADP-Ribose) polymerase inhibitor response	Gdrug response
Select item 443838	GRCh37/hg19 10q25.1-26.3(chr10:106003533-135427143)x3	ABLIM1, ABRAXAS2 +151 more	Copy number gain	See cases	GPathogenic
Select item 443323	GRCh37/hg19 10q23.32-26.3(chr10:93283493-135427143)x3	ABCC2, ABLIM1 +305 more	Copy number gain	See cases	GPathogenic
Select item 441987	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)	INA, INPP5A +721 more	Copy number gain	See cases	GPathogenic
Select item 441986	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	A1CF, ABCC2 +721 more	Copy number gain	See cases	GPathogenic
Select item 393995	GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	A1CF, ABCC2 +722 more	Copy number gain	See cases	GPathogenic
Select item 253479	GRCh37/hg19 10q24.32-26.3(chr10:103288313-135512075)x3	ABLIM1, ABRAXAS2 +201 more	Copy number gain	See cases	GPathogenic
Select item 155304	GRCh38/hg38 10q24.32-25.3(chr10:102732173-114085105)x1	LOC124416905, LOC124416906 +318 more	Copy number loss	See cases	GPathogenic
Select item 151000	GRCh38/hg38 10q25.2-25.3(chr10:110804735-114884010)x1	ABLIM1, ACSL5 +134 more	Copy number loss	See cases	GLikely pathogenic
Select item 148679	GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3	GSTO1, GSTO2 +1097 more	Copy number gain	See cases	GPathogenic
Select item 146710	GRCh38/hg38 10q25.2-25.3(chr10:112074094-115537174)x1	LOC130004765, LOC130004766 +109 more	Copy number loss	See cases	GPathogenic
Select item 144206	GRCh38/hg38 10q25.1-26.3(chr10:108102587-133620674)x3	LOC126861107, LOC128598885 +802 more	Copy number gain	See cases	GPathogenic
Select item 59707	GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3	EDRF1-AS1, EDRF1-DT +1036 more	Copy number gain	See cases	GPathogenic
Select item 58782	GRCh38/hg38 10q25.1-26.11(chr10:107191100-118761489)x1	ABLIM1, ACSL5 +308 more	Copy number loss	See cases	GPathogenic
Select item 57507	GRCh38/hg38 10q25.2-26.3(chr10:111313099-133620674)x3	ABLIM1, ABRAXAS2 +679 more	Copy number gain	See cases	GPathogenic
Select item 57116	GRCh38/hg38 10q23.33-25.3(chr10:95112607-116776637)x3	LOC130004500, LOC130004501 +821 more	Copy number gain	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 63