LYPD5[gene] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic
Select item 545227	Single allele	LOC130064626, LOC130064627 +215 more	Duplication	Schizophrenia	GLikely pathogenic
Select item 60277	GRCh38/hg38 19q13.31(chr19:43338231-43853163)x3	PHLDB3, PINLYP +55 more	Copy number gain	See cases	GUncertain significance
Select item 715325	NM_001031749.3(LYPD5):c.750A>G (p.Ser250=)	LYPD5	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2558267	NM_001031749.3(LYPD5):c.686C>T (p.Thr229Ile)	LYPD5 (T186I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370881	NM_001031749.3(LYPD5):c.656C>A (p.Thr219Asn)	LYPD5 (T176N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490872	NM_001031749.3(LYPD5):c.637T>C (p.Cys213Arg)	LYPD5 (C213R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292388	NM_001031749.3(LYPD5):c.604G>A (p.Asp202Asn)	LYPD5 (D159N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121697	NM_001031749.3(LYPD5):c.584C>G (p.Thr195Ser)	LYPD5 (T152S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121696	NM_001031749.3(LYPD5):c.556C>T (p.Arg186Trp)	LYPD5 (R186W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353590	NM_001031749.3(LYPD5):c.515T>C (p.Val172Ala)	LYPD5 (V129A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121695	NM_001031749.3(LYPD5):c.503G>A (p.Gly168Asp)	LYPD5 (G125D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121694	NM_001031749.3(LYPD5):c.497G>C (p.Gly166Ala)	LYPD5 (G123A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311407	NM_001031749.3(LYPD5):c.418G>C (p.Gly140Arg)	LYPD5 (G140R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356178	NM_001031749.3(LYPD5):c.415A>G (p.Ile139Val)	LYPD5 (I96V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3121693	NM_001031749.3(LYPD5):c.238G>C (p.Gly80Arg)	LOC130064620, LYPD5 (G80R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121692	NM_001031749.3(LYPD5):c.199C>A (p.Arg67Ser)	LOC130064620, LYPD5 (R24S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121691	NM_001031749.3(LYPD5):c.172G>T (p.Ala58Ser)	LYPD5 (A15S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292387	NM_001031749.3(LYPD5):c.144C>A (p.Ser48Arg)	LYPD5 (S5R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121690	NM_001031749.3(LYPD5):c.139C>G (p.Pro47Ala)	LYPD5 (P47A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211501	NM_001031749.3(LYPD5):c.7A>G (p.Met3Val)	LYPD5 (M3V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2425936	NC_000019.9:g.(?_44011002)_(45213778_?)dup	CADM4, CEACAM16 +37 more	Duplication	Ethylmalonic encephalopathy	GUncertain significance
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ZNF607, ZNF780A +432 more	Copy number gain	not provided	GPathogenic
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	PGLYRP1, PGLYRP2 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	TMC4, TMED1 +1364 more	Copy number gain	See cases	GPathogenic
Select item 442437	GRCh37/hg19 19q13.31-13.32(chr19:44300416-45639540)x1	APOC1, APOC2 +39 more	Copy number loss	See cases	GUncertain significance
Select item 395034	GRCh37/hg19 19q13.31(chr19:44273854-44341333)x3	KCNN4, LYPD5 +1 more	Copy number gain	See cases	GUncertain significance
Select item 253540	GRCh37/hg19 19q13.2-13.32(chr19:43013365-47241534)x1	APOC1, APOC2 +120 more	Copy number loss	See cases	GPathogenic

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Items: 28