ClinVar for Gene (Select 50856) - ClinVar

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Links from Gene

Items: 64

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3267691	NM_016184.4(CLEC4A):c.691G>A (p.Glu231Lys)	CLEC4A (E198K +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3267690	NM_016184.4(CLEC4A):c.250C>A (p.Leu84Met)	CLEC4A (L45M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3267689	NM_016184.4(CLEC4A):c.62T>C (p.Ile21Thr)	CLEC4A (I21T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3267688	NM_016184.4(CLEC4A):c.581G>A (p.Arg194His)	CLEC4A (R155H +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3267687	NM_016184.4(CLEC4A):c.61A>T (p.Ile21Phe)	CLEC4A (I21F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3244256	NC_000012.11:g.(?_7053285)_(9027607_?)del	A2ML1, ACSM4 +35 more	Deletion	Peroxisome biogenesis disorder 2B +1 more	GPathogenic
Select item 3145664	NM_016184.4(CLEC4A):c.521G>A (p.Arg174Gln)	CLEC4A (R102Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145663	NM_016184.4(CLEC4A):c.310A>T (p.Ser104Cys)	CLEC4A (S32C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145662	NM_016184.4(CLEC4A):c.292G>A (p.Val98Met)	CLEC4A (V59M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
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 2546143	NM_016184.4(CLEC4A):c.589A>T (p.Ser197Cys)	CLEC4A (S164C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521086	NM_016184.4(CLEC4A):c.590G>A (p.Ser197Asn)	CLEC4A (S125N +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2512347	NM_016184.4(CLEC4A):c.493G>A (p.Val165Met)	CLEC4A (V93M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462432	NM_016184.4(CLEC4A):c.677A>C (p.Gln226Pro)	CLEC4A (Q154P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2411542	NM_016184.4(CLEC4A):c.604C>T (p.Arg202Cys)	CLEC4A (R163C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389366	NM_016184.4(CLEC4A):c.302C>T (p.Thr101Ile)	CLEC4A (T101I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364398	NM_016184.4(CLEC4A):c.580C>T (p.Arg194Cys)	CLEC4A (R194C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331963	NM_016184.4(CLEC4A):c.8C>T (p.Ser3Leu)	CLEC4A (S3L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309191	NM_016184.4(CLEC4A):c.625C>T (p.Arg209Cys)	CLEC4A (R170C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286864	NM_016184.4(CLEC4A):c.275T>C (p.Val92Ala)	CLEC4A (V92A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258198	NM_016184.4(CLEC4A):c.673C>T (p.Pro225Ser)	CLEC4A (P225S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206404	NM_016184.4(CLEC4A):c.647G>A (p.Gly216Asp)	CLEC4A (G144D +3 more)	Single nucleotide variant (missense variant)	not specified	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 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 815493	GRCh37/hg19 12p13.33-q11(chr12:274676-37869301)x4	ART4, DYRK4 +278 more	Copy number gain	not provided	GPathogenic
Select item 732592	NM_016184.4(CLEC4A):c.712T>C (p.Ter238Arg)	CLEC4A	Single nucleotide variant (stop lost)	not provided	GBenign
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 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 619591	NC_000012.12:g.(1_3750000)_(5250000_9000000)del	GAPDH, GAU1 +477 more	Deletion	Tumoral calcinosis, hyperphosphatemic, familial, 1	Gnot provided
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 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 153962	GRCh38/hg38 12p13.33-11.1(chr12:64620-34682902)x4	CLEC12A, CLEC12A-AS1 +1258 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 151004	GRCh38/hg38 12p13.33-11.1(chr12:54427-34608071)x4	TAS2R9, TEAD4 +1258 more	Copy number gain	See cases	GPathogenic
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	FERRY3, FGD4 +4837 more	Copy number gain	See cases	GPathogenic
Select item 150653	GRCh38/hg38 12p13.31(chr12:7850905-8455624)x1	C3AR1, CLEC4A +39 more	Copy number loss	See cases	GLikely benign
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 148626	GRCh38/hg38 12p13.33-12.3(chr12:2871741-14987348)x3	LOC130007190, LOC130007191 +698 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 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 59795	GRCh38/hg38 12p13.33-12.1(chr12:80412-25470329)x3	A2M, A2M-AS1 +1009 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

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Links from Gene

Items: 64