PLCXD3[gene] - ClinVar

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Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 149824	GRCh38/hg38 5p15.33-q13.3(chr5:22149-74412725)x3	ACTBL2, ADAMTS12 +1445 more	Copy number gain	See cases	GPathogenic
Select item 146130	GRCh38/hg38 5p15.33-11(chr5:49978-46114984)x3	ADAMTS12, ADAMTS16 +953 more	Copy number gain	See cases	GPathogenic
Select item 58067	GRCh38/hg38 5p15.33-12(chr5:54839-45649861)x3	ADAMTS12, ADAMTS16 +952 more	Copy number gain	See cases	GPathogenic
Select item 2683745	GRCh38/hg38 5p13.3-12(chr5:29299893-45899898)x3	AGXT2, LOC121725200 +385 more	Copy number gain	See cases	GLikely pathogenic
Select item 148227	GRCh38/hg38 5p13.2-q12.1(chr5:35201559-61903141)x3	LINC02057, LINC02101 +518 more	Copy number gain	See cases	GPathogenic
Select item 58092	GRCh38/hg38 5p13.2-12(chr5:35700480-45260029)x3	LOC126807367, LOC126807368 +254 more	Copy number gain	See cases	GPathogenic
Select item 58093	GRCh38/hg38 5p13.2-q11.1(chr5:36374107-51103841)x3	ANXA2R, ANXA2R-AS1 +245 more	Copy number gain	See cases	GPathogenic
Select item 2258321	NM_001005473.3(PLCXD3):c.917C>T (p.Thr306Ile)	PLCXD3 (T306I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273159	NM_001005473.3(PLCXD3):c.785G>A (p.Ser262Asn)	PLCXD3 (S262N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569921	NM_001005473.3(PLCXD3):c.758C>G (p.Ala253Gly)	PLCXD3 (A253G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214611	NM_001005473.3(PLCXD3):c.734C>G (p.Ser245Cys)	PLCXD3 (S245C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214610	NM_001005473.3(PLCXD3):c.667G>A (p.Glu223Lys)	PLCXD3 (E223K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532987	NM_001005473.3(PLCXD3):c.663C>G (p.Asp221Glu)	PLCXD3 (D221E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611528	NM_001005473.3(PLCXD3):c.625G>A (p.Gly209Arg)	PLCXD3 (G209R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283449	NM_001005473.3(PLCXD3):c.564C>G (p.Asp188Glu)	PLCXD3 (D188E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3307405	NM_001005473.3(PLCXD3):c.493A>G (p.Ile165Val)	PLCXD3 (I165V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214609	NM_001005473.3(PLCXD3):c.458A>G (p.Tyr153Cys)	PLCXD3 (Y153C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217698	NM_001005473.3(PLCXD3):c.407A>G (p.His136Arg)	PLCXD3 (H136R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214608	NM_001005473.3(PLCXD3):c.386A>G (p.Asn129Ser)	PLCXD3 (N129S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214607	NM_001005473.3(PLCXD3):c.317C>A (p.Pro106His)	PLCXD3 (P106H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605270	NM_001005473.3(PLCXD3):c.253A>G (p.Thr85Ala)	PLCXD3 (T85A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356637	NM_001005473.3(PLCXD3):c.184G>A (p.Val62Ile)	PLCXD3 (V62I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808669	GRCh37/hg19 5p13.3-11(chr5:29348753-46389339)x3	ADAMTS12, AGXT2 +71 more	Copy number gain	not provided	GPathogenic
Select item 1705919	GRCh37/hg19 5p13.2-11(chr5:36053583-46389339)x3	ANXA2R, C5orf34 +45 more	Copy number gain	musculoskeletal system issues	GPathogenic
Select item 1527153	GRCh37/hg19 5p14.1-11(chr5:26382110-46389339)	ADAMTS12, AGXT2 +72 more	Copy number gain	not specified	GPathogenic
Select item 1180548	GRCh37/hg19 5p13.2-11(chr5:34984696-46405042)x3	AGXT2, ANXA2R +51 more	Copy number gain	not provided	GPathogenic
Select item 1012370	GRCh37/hg19 5p13.3-12(chr5:29081195-45294031)x3	ADAMTS12, AGXT2 +71 more	Copy number gain	See cases	GPathogenic
Select item 979500	GRCh37/hg19 5p13.1(chr5:41087704-41604627)x1	PLCXD3, C6	Copy number loss	not provided	GUncertain significance
Select item 814684	GRCh37/hg19 5p13.1-q11.1(chr5:38432180-49441945)x3	GHR, CARD6 +31 more	Copy number gain	not provided	GPathogenic
Select item 687304	GRCh37/hg19 5p13.2-11(chr5:34453883-46389339)x3	AGXT2, ANXA2R +56 more	Copy number gain	not provided	GPathogenic
Select item 635930	Single allele	C5orf24, C5orf34 +600 more	Deletion	Neurodevelopmental disorder	GUncertain significance
Select item 563053	GRCh37/hg19 5p14.1-12(chr5:27227243-45685844)x3	C1QTNF3, C5orf22 +71 more	Copy number gain	not provided	GPathogenic
Select item 442809	GRCh37/hg19 5p14.2-11(chr5:24281195-46389339)x3	ADAMTS12, AGXT2 +73 more	Copy number gain	See cases	GLikely pathogenic
Select item 442431	GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1	DHFR, DHX29 +738 more	Copy number loss	See cases	GPathogenic
Select item 441920	GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)	ABLIM3, ACOT12 +870 more	Copy number gain	See cases	GPathogenic
Select item 441919	GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3	ABLIM3, ACOT12 +870 more	Copy number gain	See cases	GPathogenic
Select item 253597	GRCh37/hg19 5p15.2-12(chr5:13461664-46098927)x3	RXFP3, GDNF +89 more	Copy number gain	See cases	GPathogenic

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Items: 37