DCP1B[gene] - ClinVar - NCBI

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	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 146024	GRCh38/hg38 12p13.33-13.31(chr12:45740-6945196)x3	ACRBP, ADIPOR2 +348 more	Copy number gain	See cases	GPathogenic
Select item 152732	GRCh38/hg38 12p13.33-13.32(chr12:54427-3639603)x1	ADIPOR2, B4GALNT3 +142 more	Copy number loss	See cases	GPathogenic
Select item 152450	GRCh38/hg38 12p13.33-13.32(chr12:54427-4004912)x1	ADIPOR2, B4GALNT3 +147 more	Copy number loss	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 147092	GRCh38/hg38 12p13.33(chr12:54452-2558097)x1	ADIPOR2, B4GALNT3 +101 more	Copy number loss	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 149561	GRCh38/hg38 12p13.33-13.32(chr12:80412-4420585)x1	ADIPOR2, B4GALNT3 +170 more	Copy number loss	See cases	GPathogenic
Select item 148625	GRCh38/hg38 12p13.33(chr12:80412-2850599)x1	ADIPOR2, B4GALNT3 +114 more	Copy number loss	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 154528	GRCh38/hg38 12p13.33(chr12:121255-3003320)x1	ADIPOR2, B4GALNT3 +123 more	Copy number loss	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 57044	GRCh38/hg38 12p13.33-13.32(chr12:121255-3968447)x1	ADIPOR2, B4GALNT3 +146 more	Copy number loss	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 147690	GRCh38/hg38 12p13.33-13.31(chr12:199896-5807366)x1	ADIPOR2, AKAP3 +218 more	Copy number loss	See cases	GPathogenic
Select item 59798	GRCh38/hg38 12p13.33-13.32(chr12:199896-3284963)x3	ADIPOR2, B4GALNT3 +126 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 155290	GRCh38/hg38 12p13.33-13.31(chr12:418421-6235914)x3	ADIPOR2, AKAP3 +223 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 58206	GRCh38/hg38 12p13.33(chr12:1453550-2575642)x3	ADIPOR2, CACNA1C +49 more	Copy number gain	See cases	GUncertain significance
Select item 146064	GRCh38/hg38 12p13.33(chr12:1678885-2546760)x3	ADIPOR2, CACNA1C +22 more	Copy number gain	See cases	GUncertain significance
Select item 2216483	NM_152640.5(DCP1B):c.1834G>A (p.Ala612Thr)	DCP1B (A612T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080572	NM_152640.5(DCP1B):c.1825A>T (p.Thr609Ser)	DCP1B (T609S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529686	NM_152640.5(DCP1B):c.1793A>C (p.Asn598Thr)	DCP1B (N598T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080571	NM_152640.5(DCP1B):c.1706C>T (p.Pro569Leu)	DCP1B (P569L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 776685	NM_152640.5(DCP1B):c.1701G>A (p.Pro567=)	DCP1B	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3080570	NM_152640.5(DCP1B):c.1630G>A (p.Gly544Ser)	DCP1B (G544S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 712109	NM_152640.5(DCP1B):c.1629C>T (p.Ser543=)	DCP1B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2591783	NM_152640.5(DCP1B):c.1606G>A (p.Val536Ile)	DCP1B (V536I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080569	NM_152640.5(DCP1B):c.1600A>C (p.Thr534Pro)	DCP1B (T534P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3271108	NM_152640.5(DCP1B):c.1541G>A (p.Arg514His)	DCP1B (R514H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331904	NM_152640.5(DCP1B):c.1457C>T (p.Thr486Ile)	DCP1B (T486I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513770	NM_152640.5(DCP1B):c.1454G>C (p.Gly485Ala)	DCP1B (G485A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080568	NM_152640.5(DCP1B):c.1409G>A (p.Arg470Gln)	DCP1B (R470Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619530	NM_152640.5(DCP1B):c.1379A>G (p.Gln460Arg)	DCP1B (Q460R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411528	NM_152640.5(DCP1B):c.1366C>T (p.Leu456Phe)	DCP1B (L456F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299298	NM_152640.5(DCP1B):c.1206G>C (p.Gln402His)	DCP1B (Q402H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390251	NM_152640.5(DCP1B):c.1177C>T (p.Pro393Ser)	DCP1B (P393S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2281712	NM_152640.5(DCP1B):c.1160C>T (p.Ala387Val)	DCP1B (A387V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540547	NM_152640.5(DCP1B):c.1155C>G (p.Ser385Arg)	DCP1B (S385R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 781059	NM_152640.5(DCP1B):c.1151G>A (p.Arg384His)	DCP1B (R384H)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2273883	NM_152640.5(DCP1B):c.1111C>T (p.Pro371Ser)	DCP1B (P371S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2388475	NM_152640.5(DCP1B):c.1080G>C (p.Gln360His)	DCP1B (Q360H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080567	NM_152640.5(DCP1B):c.1057C>A (p.Gln353Lys)	DCP1B (Q353K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395064	NM_152640.5(DCP1B):c.1030C>T (p.Arg344Cys)	DCP1B (R344C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509890	NM_152640.5(DCP1B):c.1016A>C (p.Asn339Thr)	DCP1B (N339T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352546	NM_152640.5(DCP1B):c.1016A>T (p.Asn339Ile)	DCP1B (N339I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215819	NM_152640.5(DCP1B):c.986C>T (p.Thr329Ile)	DCP1B (T329I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080576	NM_152640.5(DCP1B):c.941G>A (p.Arg314Gln)	DCP1B (R314Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2565939	NM_152640.5(DCP1B):c.910C>T (p.Leu304Phe)	DCP1B (L304F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524853	NM_152640.5(DCP1B):c.904G>A (p.Ala302Thr)	DCP1B (A302T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 773020	NM_152640.5(DCP1B):c.902G>C (p.Ser301Thr)	DCP1B (S301T)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2332758	NM_152640.5(DCP1B):c.894G>A (p.Met298Ile)	DCP1B (M298I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2287891	NM_152640.5(DCP1B):c.740C>T (p.Pro247Leu)	DCP1B (P247L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2348807	NM_152640.5(DCP1B):c.632G>A (p.Arg211His)	DCP1B (R211H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2410167	NM_152640.5(DCP1B):c.570C>G (p.Ile190Met)	DCP1B (I190M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339090	NM_152640.5(DCP1B):c.532T>G (p.Cys178Gly)	DCP1B (C178G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3271109	NM_152640.5(DCP1B):c.476T>G (p.Val159Gly)	DCP1B (V159G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2230347	NM_152640.5(DCP1B):c.424A>G (p.Thr142Ala)	DCP1B (T142A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3080574	NM_152640.5(DCP1B):c.420G>C (p.Gln140His)	DCP1B (Q140H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2570815	NM_152640.5(DCP1B):c.294T>G (p.Pro98=)	CACNA1C, DCP1B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3080573	NM_152640.5(DCP1B):c.212G>A (p.Gly71Glu)	CACNA1C, DCP1B (G71E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3341601	NM_152640.5(DCP1B):c.93C>A (p.Ile31=)	CACNA1C, DCP1B	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2283727	NM_152640.5(DCP1B):c.80A>G (p.Tyr27Cys)	CACNA1C, DCP1B (Y27C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3080575	NM_152640.5(DCP1B):c.7G>C (p.Ala3Pro)	CACNA1C, DCP1B (A3P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
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 3024578	GRCh37/hg19 12p13.33(chr12:922808-2129821)x1	ADIPOR2, CACNA2D4 +7 more	Copy number loss	not provided	GLikely pathogenic
Select item 2685429	GRCh37/hg19 12p13.33-13.32(chr12:191243-5332596)x1	ADIPOR2, AKAP3 +40 more	Copy number loss	not provided	GPathogenic
Select item 2685428	GRCh37/hg19 12p13.33(chr12:173787-2431561)x1	ADIPOR2, B4GALNT3 +16 more	Copy number loss	not provided	GUncertain significance
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 2427496	NC_000012.11:g.(?_862732)_(2800365_?)dup	ADIPOR2, CACNA1C +8 more	Duplication	not provided	GUncertain significance
Select item 2423370	NC_000012.11:g.(?_2016586)_(2558301_?)dup	CACNA1C, CACNA2D4 +1 more	Duplication	Long QT syndrome	GUncertain significance
Select item 2423369	NC_000012.11:g.(?_1949885)_(2764424_?)dup	CACNA1C, CACNA2D4 +1 more	Duplication	Long QT syndrome	GUncertain significance
Select item 1809216	GRCh37/hg19 12p13.33(chr12:817514-2205439)x1	ADIPOR2, CACNA1C +8 more	Copy number loss	not provided	GPathogenic
Select item 1808497	GRCh37/hg19 12p13.33(chr12:2056363-2801698)x1	CACNA1C, DCP1B	Copy number loss	not provided	GUncertain significance
Select item 1808214	GRCh37/hg19 12p13.33(chr12:2019716-2674054)x3	CACNA1C, CACNA2D4 +1 more	Copy number gain	not provided	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 1527676	GRCh37/hg19 12p13.33(chr12:2019715-2674054)x3	CACNA1C, CACNA2D4 +1 more	Copy number gain	not specified	GUncertain significance
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 1434649	NC_000012.11:g.(?_1949885)_(2229616_?)dup	CACNA1C, CACNA2D4 +1 more	Duplication	not provided	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 1180524	GRCh37/hg19 12p13.33-13.31(chr12:189145-7730395)x3	CRACR2A, ERC1 +93 more	Copy number gain	not provided	GPathogenic
Select item 979958	GRCh37/hg19 12p13.33-13.32(chr12:191242-4683495)x1	ADIPOR2, B4GALNT3 +33 more	Copy number loss	not provided	GPathogenic
Select item 979957	GRCh37/hg19 12p13.33(chr12:2019715-2674054)x3	CACNA1C, CACNA2D4 +1 more	Copy number gain	not provided	GUncertain significance
Select item 833161	NC_000012.12:g.(?_1909906)_(2556977_?)dup	DCP1B, CACNA1C +1 more	Duplication	not provided	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 688469	GRCh37/hg19 12p13.33(chr12:1436977-2156672)x3	ADIPOR2, CACNA2D4 +5 more	Copy number gain	not provided	GUncertain significance
Select item 687115	GRCh37/hg19 12p13.33-13.31(chr12:173786-6346092)x1	ADIPOR2, AKAP3 +44 more	Copy number loss	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 685532	GRCh37/hg19 12p13.33(chr12:2078015-2316617)x3	CACNA1C, DCP1B	Copy number gain	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

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