CLEC4C[gene] - ClinVar

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Items: 68

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 619591	NC_000012.12:g.(1_3750000)_(5250000_9000000)del	GAPDH, GAU1 +477 more	Deletion	Tumoral calcinosis, hyperphosphatemic, familial, 1	Gnot provided
Select item 151004	GRCh38/hg38 12p13.33-11.1(chr12:54427-34608071)x4	TAS2R9, TEAD4 +1258 more	Copy number gain	See cases	GPathogenic
Select item 153962	GRCh38/hg38 12p13.33-11.1(chr12:64620-34682902)x4	CLEC12A, CLEC12A-AS1 +1258 more	Copy number gain	See cases	GPathogenic
Select item 59794	GRCh38/hg38 12p13.33-11.1(chr12:77187-34380176)x3	LOC126861410, LOC126861411 +1258 more	Copy number gain	See cases	GPathogenic
Select item 59795	GRCh38/hg38 12p13.33-12.1(chr12:80412-25470329)x3	A2M, A2M-AS1 +1009 more	Copy number gain	See cases	GPathogenic
Select item 147419	GRCh38/hg38 12p13.33-11.1(chr12:121255-34603274)x3	LOC130007230, LOC130007231 +1257 more	Copy number gain	See cases	GPathogenic
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	ACAD10, ACADS +4836 more	Copy number gain	See cases	GPathogenic
Select item 150158	GRCh38/hg38 12p13.33-11.1(chr12:121271-34603261)x3	LOC126861494, LOC126861495 +1257 more	Copy number gain	See cases	GPathogenic
Select item 59799	GRCh38/hg38 12p13.33-11.1(chr12:212976-33926913)x4	CACNA1C-AS2, CACNA1C-AS4 +1242 more	Copy number gain	See cases	GPathogenic
Select item 153563	GRCh38/hg38 12p13.33-12.2(chr12:1258274-20657577)x3	A2M, A2M-AS1 +853 more	Copy number gain	See cases	GPathogenic
Select item 148626	GRCh38/hg38 12p13.33-12.3(chr12:2871741-14987348)x3	LOC130007190, LOC130007191 +698 more	Copy number gain	See cases	GPathogenic
Select item 2546370	NM_001371390.1(CLEC4C):c.605A>G (p.Gln202Arg)	CLEC4C (Q202R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340368	NM_001371390.1(CLEC4C):c.557G>A (p.Arg186His)	CLEC4C (R149H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145670	NM_001371390.1(CLEC4C):c.556C>T (p.Arg186Cys)	CLEC4C (R155C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145669	NM_001371390.1(CLEC4C):c.484A>G (p.Asn162Asp)	CLEC4C (N131D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267692	NM_001371390.1(CLEC4C):c.449G>A (p.Arg150Gln)	CLEC4C (R119Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267694	NM_001371390.1(CLEC4C):c.431T>C (p.Leu144Pro)	CLEC4C (L144P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 768512	NM_001371390.1(CLEC4C):c.366C>A (p.Asn122Lys)	CLEC4C, LOC129390394 (N85K +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2342372	NM_001371390.1(CLEC4C):c.229A>G (p.Ile77Val)	CLEC4C (I46V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145666	NM_001371390.1(CLEC4C):c.193C>T (p.His65Tyr)	CLEC4C (H65Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 727182	NM_001371390.1(CLEC4C):c.172T>G (p.Leu58Val)	CLEC4C (L27V +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2469288	NM_001371390.1(CLEC4C):c.169A>C (p.Lys57Gln)	CLEC4C (K57Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145665	NM_001371390.1(CLEC4C):c.141G>T (p.Met47Ile)	CLEC4C (M47I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145672	NM_001371390.1(CLEC4C):c.91C>A (p.Leu31Ile)	CLEC4C (L31I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145671	NM_001371390.1(CLEC4C):c.79G>A (p.Val27Ile)	CLEC4C (V27I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145668	NM_001371390.1(CLEC4C):c.40C>T (p.Leu14Phe)	CLEC4C (L14F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145667	NM_001371390.1(CLEC4C):c.35A>G (p.Lys12Arg)	CLEC4C (K12R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509065	NM_001371390.1(CLEC4C):c.4G>A (p.Val2Met)	CLEC4C (V2M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 147698	GRCh38/hg38 12p13.31(chr12:7747398-7919345)x3	CLEC4C, LOC108942766 +11 more	Copy number gain	See cases	GBenign
Select item 147678	GRCh38/hg38 12p13.31(chr12:7747398-7936064)x3	CLEC4C, LOC108942766 +11 more	Copy number gain	See cases	GBenign
Select item 3244256	NC_000012.11:g.(?_7053285)_(9027607_?)del	A2ML1, ACSM4 +35 more	Deletion	Peroxisome biogenesis disorder 2B +1 more	GPathogenic
Select item 3063250	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835641)x3	A2M, A2ML1 +278 more	Copy number gain	not specified	GPathogenic
Select item 2671607	Single allele	FGD4, FGF23 +278 more	Duplication	not provided	GPathogenic
Select item 2445417	GRCh37/hg19 12p13.33-11.1(chr12:176047-34179852)x4	DENND5B, DERA +278 more	Copy number gain	Pallister-Killian syndrome	GPathogenic
Select item 2423987	NC_000012.11:g.(?_4368352)_(9027607_?)dup	A2ML1, ACRBP +85 more	Duplication	Lymphoproliferative syndrome 2	GUncertain significance
Select item 1807708	GRCh37/hg19 12p13.33-13.31(chr12:173787-8320544)x3	ACRBP, ACSM4 +105 more	Copy number gain	not provided	GPathogenic
Select item 1527672	GRCh37/hg19 12p13.33-q11(chr12:173786-37869301)	C3AR1, CACNA1C +278 more	Copy number gain	not specified	GPathogenic
Select item 1527671	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)	A2M, A2ML1 +278 more	Copy number gain	not specified	GPathogenic
Select item 1527669	GRCh37/hg19 12p13.33-12.1(chr12:173786-25286865)	A2ML1, ABCC9 +235 more	Copy number gain	not specified	GPathogenic
Select item 1473612	NC_000012.11:g.(?_6438478)_(8756953_?)dup	ACRBP, ACSM4 +64 more	Duplication	not provided	GUncertain significance
Select item 1409561	NC_000012.11:g.(?_6438478)_(8248686_?)dup	PEX5, PHB2 +57 more	Duplication	Temtamy syndrome	GUncertain significance
Select item 1373618	NC_000012.11:g.(?_6978008)_(9010204_?)dup	C12orf57, ATN1 +40 more	Duplication	Peroxisome biogenesis disorder 2B	GUncertain significance
Select item 1330180	GRCh37/hg19 12p13.33-13.31(chr12:146240-8330229)x3	CLEC4A, LRRC23 +106 more	Copy number gain	Single transverse palmar crease +6 more	GPathogenic
Select item 1004385	NC_000012.11:g.(?_6945914)_(9027627_?)dup	C1RL, C1S +44 more	Duplication	Klippel-Feil syndrome 3, autosomal dominant	GUncertain significance
Select item 979952	GRCh37/hg19 12p13.31(chr12:7755907-8436318)x3	FAM90A1, NECAP1 +12 more	Copy number gain	not provided	GLikely benign
Select item 832123	NC_000012.12:g.(?_7689858)_(8096110_?)dup	C3AR1, CLEC4C +8 more	Duplication	Developmental and epileptic encephalopathy, 21	GUncertain significance
Select item 830465	NC_000012.11:g.(?_6945914)_(8248706_?)dup	ACSM4, APOBEC1 +34 more	Duplication	Temtamy syndrome	GUncertain significance
Select item 815493	GRCh37/hg19 12p13.33-q11(chr12:274676-37869301)x4	ART4, DYRK4 +278 more	Copy number gain	not provided	GPathogenic
Select item 686501	GRCh37/hg19 12p13.33-11.1(chr12:173786-34496628)x3	CLEC1B, CLEC2A +278 more	Copy number gain	not provided	GPathogenic
Select item 685635	GRCh37/hg19 12p13.33-13.31(chr12:173786-8393815)x3	ACRBP, ACSM4 +107 more	Copy number gain	not provided	GPathogenic
Select item 685572	GRCh37/hg19 12p13.31(chr12:7815254-8013345)x1	APOBEC1, CLEC4C +5 more	Copy number loss	not provided	GUncertain significance
Select item 625811	GRCh37/hg19 12p13.33-13.31(chr12:189216-8185497)	ACRBP, ACSM4 +102 more	Copy number gain	not provided	GPathogenic
Select item 625810	GRCh37/hg19 12p13.33-13.31(chr12:237588-8278292)	ACRBP, ACSM4 +105 more	Copy number gain	not provided	GPathogenic
Select item 625809	GRCh37/hg19 12p13.33-12.3(chr12:189216-15001420)	A2M, A2ML1 +193 more	Copy number gain	not provided	GPathogenic
Select item 563991	GRCh37/hg19 12p13.33-q11(chr12:173786-37869107)x3	A2M, A2ML1 +278 more	Copy number gain	not provided	GPathogenic
Select item 563990	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x3	A2M, A2ML1 +278 more	Copy number gain	not provided	GPathogenic
Select item 563989	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x2,3	A2M, A2ML1 +278 more	Copy number gain	not provided	GPathogenic
Select item 563988	GRCh37/hg19 12p13.33-13.31(chr12:191242-8122785)x3	ACRBP, ACSM4 +101 more	Copy number gain	not provided	GPathogenic
Select item 443532	GRCh37/hg19 12p13.33-11.22(chr12:173786-28219229)x3	A2M, A2ML1 +256 more	Copy number gain	See cases	GPathogenic
Select item 442150	GRCh37/hg19 12p13.33-11.1(chr12:565369-34835837)x3	KCNA6, KCNJ8 +273 more	Copy number gain	See cases	GLikely pathogenic
Select item 441984	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	SLC15A5, SLC16A7 +1006 more	Copy number gain	See cases	GPathogenic
Select item 441983	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	A2M, A2ML1 +1006 more	Copy number gain	See cases	GPathogenic
Select item 441823	GRCh37/hg19 12p13.33-13.2(chr12:173786-11677456)x3	A2M, A2ML1 +166 more	Copy number gain	See cases	GPathogenic
Select item 395673	GRCh37/hg19 12p13.33-11.1(chr12:189578-34756150)	A2M, A2ML1 +278 more	Copy number gain	See cases	GPathogenic
Select item 268075	GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	GALNT8, H2AJ +1007 more	Copy number gain	See cases	GPathogenic
Select item 253582	GRCh37/hg19 12p13.33-11.1(chr12:148034-34178799)x4	ACSM4, CCND2 +278 more	Copy number gain	See cases	GPathogenic
Select item 253493	GRCh37/hg19 12p13.33-11.1(chr12:89061-34178799)x3	A2M, A2ML1 +278 more	Copy number gain	See cases	GPathogenic
Select item 221847	GRCh37/hg19 12p13.31(chr12:7895024-8014573)x3	CLEC4C, NANOG +2 more	Copy number gain	Premature ovarian failure	GBenign

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Items: 68