APOD[gene] - ClinVar

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Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145614	GRCh38/hg38 3q13.11-29(chr3:103426882-198110178)x3	BPESC1, BTLA +2645 more	Copy number gain	See cases	GPathogenic
Select item 57983	GRCh38/hg38 3q24-29(chr3:147521892-198096565)x3	BDH1, C3orf33 +1449 more	Copy number gain	See cases	GPathogenic
Select item 150609	GRCh38/hg38 3q25.1-29(chr3:152100512-198118383)x3	LINC00578, LINC00880 +1317 more	Copy number gain	See cases	GPathogenic
Select item 154213	GRCh38/hg38 3q25.31-29(chr3:156118441-198125115)x3	PAK2, PARL +1246 more	Copy number gain	See cases	GPathogenic
Select item 152257	GRCh38/hg38 3q25.31-29(chr3:156321878-198113452)x3	LOC129937828, LOC129937829 +1244 more	Copy number gain	See cases	GPathogenic
Select item 57984	GRCh38/hg38 3q25.31-29(chr3:157293378-198134727)x3	LOC129938023, LOC129938024 +1200 more	Copy number gain	See cases	GPathogenic
Select item 155627	GRCh38/hg38 3q26.1-29(chr3:166137209-198125115)x3	ABCC5, ABCC5-AS1 +1064 more	Copy number gain	See cases	GPathogenic
Select item 148012	GRCh38/hg38 3q26.2-29(chr3:168167568-198110178)x3	ABCC5, ABCC5-AS1 +1041 more	Copy number gain	See cases	GPathogenic
Select item 149685	GRCh38/hg38 3q26.32-29(chr3:176168525-198118383)x3	ALG3, AP2M1 +867 more	Copy number gain	See cases	GPathogenic
Select item 148947	GRCh38/hg38 3q26.32-29(chr3:176439911-198118383)x3	ABCC5, ABCC5-AS1 +866 more	Copy number gain	See cases	GPathogenic
Select item 57868	GRCh38/hg38 3q27.2-29(chr3:185485849-198110178)x1	LOC110121069, LOC110121110 +557 more	Copy number loss	See cases	GPathogenic
Select item 57997	GRCh38/hg38 3q28-29(chr3:189265371-198110178)x3	ACAP2, APOD +411 more	Copy number gain	See cases	GPathogenic
Select item 57998	GRCh38/hg38 3q28-29(chr3:190667663-198110178)x3	ACAP2, APOD +375 more	Copy number gain	See cases	GPathogenic
Select item 148761	GRCh38/hg38 3q29(chr3:192752937-198118383)x3	ACAP2, APOD +337 more	Copy number gain	See cases	GPathogenic
Select item 155434	GRCh38/hg38 3q29(chr3:193704605-198125115)x3	ACAP2, APOD +313 more	Copy number gain	See cases	GPathogenic
Select item 149477	GRCh38/hg38 3q29(chr3:194296197-198110198)x3	SENP5, XXYLT1 +273 more	Copy number gain	See cases	GPathogenic
Select item 147306	GRCh38/hg38 3q29(chr3:194338534-197693741)x1	ACAP2, APOD +239 more	Copy number loss	See cases	GPathogenic
Select item 58000	GRCh38/hg38 3q29(chr3:194424496-198168758)x3	ACAP2, APOD +264 more	Copy number gain	See cases	GPathogenic
Select item 147389	GRCh38/hg38 3q29(chr3:195147600-195711857)x3	ACAP2, APOD +30 more	Copy number gain	See cases	GUncertain significance
Select item 149646	GRCh38/hg38 3q29(chr3:195537024-195730806)x1	APOD, LOC105374297 +12 more	Copy number loss	See cases	GLikely benign
Select item 149645	GRCh38/hg38 3q29(chr3:195537024-195730806)x3	APOD, LOC105374297 +12 more	Copy number gain	See cases	GLikely benign
Select item 146658	GRCh38/hg38 3q29(chr3:195537179-195732718)x3	APOD, LOC105374297 +12 more	Copy number gain	See cases	GBenign
Select item 147685	GRCh38/hg38 3q29(chr3:195537187-195736631)x3	APOD, LOC105374297 +12 more	Copy number gain	See cases	GBenign
Select item 2355910	NM_001647.4(APOD):c.559A>G (p.Lys187Glu)	APOD (K187E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3038449	NM_001647.4(APOD):c.383A>G (p.Tyr128Cys)	APOD (Y128C)	Single nucleotide variant (missense variant)	APOD-related condition	GLikely benign
Select item 2402066	NM_001647.4(APOD):c.370G>A (p.Asp124Asn)	APOD (D124N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2464879	NM_001647.4(APOD):c.350C>T (p.Pro117Leu)	APOD (P117L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355698	NM_001647.4(APOD):c.304C>G (p.Pro102Ala)	APOD (P102A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2654366	NM_001647.4(APOD):c.226G>A (p.Val76Met)	APOD (V76M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2518975	NM_001647.4(APOD):c.178C>T (p.Arg60Cys)	APOD (R60C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3044850	NM_001647.4(APOD):c.166T>G (p.Phe56Val)	APOD (F56V)	Single nucleotide variant (missense variant)	APOD-related condition	GBenign
Select item 748647	NM_001647.4(APOD):c.165C>A (p.Thr55=)	APOD	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2348249	NM_001647.4(APOD):c.142G>A (p.Glu48Lys)	APOD (E48K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2368269	NM_001647.4(APOD):c.85C>T (p.Pro29Ser)	APOD (P29S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 769625	NM_001647.4(APOD):c.44T>C (p.Phe15Ser)	APOD (F15S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2240799	NM_001647.4(APOD):c.31C>G (p.Leu11Val)	APOD (L11V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2685950	GRCh37/hg19 3q29(chr3:195244842-195769200)x3	APOD, MIR570 +5 more	Copy number gain	not provided	GUncertain significance
Select item 2671619	Single allele	ABCC5, ABCF3 +145 more	Duplication	not provided	GPathogenic
Select item 2671595	Single allele	AADAC, AADACL2 +286 more	Duplication	not provided	GPathogenic
Select item 1808252	GRCh37/hg19 3q29(chr3:195279004-195743958)x4	APOD, TNK2 +4 more	Copy number gain	not provided	GUncertain significance
Select item 1707630	GRCh37/hg19 3q26.31-29(chr3:171558472-197871052)x3	CCDC50, MELTF +155 more	Copy number gain	Isolated anorectal malformation	GLikely pathogenic
Select item 1707428	GRCh37/hg19 3q27.1-29(chr3:183498520-197851986)x3	ABCC5, ABCF3 +118 more	Copy number gain	See cases	GPathogenic
Select item 1340876	GRCh37/hg19 3q29(chr3:195279003-195718752)x3	APOD, MIR570 +4 more	Copy number gain	not provided	GUncertain significance
Select item 1330171	GRCh37/hg19 3q29(chr3:194790394-197961930)x3	ACAP2, APOD +35 more	Copy number gain	Chromosome 3q29 microdeletion syndrome	GUncertain significance
Select item 1328450	GRCh37/hg19 3q28-29(chr3:191866466-197842171)x1	ACAP2, APOD +48 more	Copy number loss	not provided	GPathogenic
Select item 1326307	GRCh37/hg19 3q28-29(chr3:189608636-197532175)x1	OPA1, OSTN +56 more	Copy number loss	3q28q29 deletion syndrome	GPathogenic
Select item 988913	GRCh37/hg19 3q29(chr3:194498718-196196789)x1	ACAP2, APOD +15 more	Copy number loss	not provided	GUncertain significance
Select item 980655	GRCh37/hg19 3q29(chr3:195068028-197851986)x3	DLG1, PPP1R2 +33 more	Copy number gain	not provided	GPathogenic
Select item 686149	GRCh37/hg19 3q29(chr3:195279196-196022437)x3	APOD, DYNLT2B +9 more	Copy number gain	not provided	GUncertain significance
Select item 638098	GRCh37/hg19 3q28-29(chr3:188386566-197838262)x3	GMNC, GP5 +62 more	Copy number gain	See cases	GPathogenic
Select item 562857	GRCh37/hg19 3q28-29(chr3:191593619-197851986)x3	MB21D2, MUC4 +48 more	Copy number gain	not provided	GPathogenic
Select item 562855	GRCh37/hg19 3q28-29(chr3:187913567-197851986)x3	TMEM44, GP5 +62 more	Copy number gain	not provided	GPathogenic
Select item 562852	GRCh37/hg19 3q27.3-29(chr3:186374365-197851986)x3	PCYT1A, TNK2-AS1 +77 more	Copy number gain	not provided	GPathogenic
Select item 562850	GRCh37/hg19 3q27.1-29(chr3:184003967-197851986)x3	FYTTD1, FAM43A +103 more	Copy number gain	not provided	GPathogenic
Select item 562847	GRCh37/hg19 3q26.33-29(chr3:182539234-197851986)x3	PPP1R2, TBCCD1 +126 more	Copy number gain	not provided	GPathogenic
Select item 442401	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	FBXL2, FBXO40 +1054 more	Copy number gain	See cases	GPathogenic
Select item 442400	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	A4GNT, AADAC +1054 more	Copy number gain	See cases	GPathogenic
Select item 393885	GRCh37/hg19 3q25.32-29(chr3:158980631-197766890)x3	ABCC5, ABCF3 +198 more	Copy number gain	See cases	GPathogenic

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Items: 58