TRIB2[gene] - ClinVar

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Items: 48

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 153520	GRCh38/hg38 2p25.3-23.3(chr2:12770-25039694)x3	LOC129933244, LOC129933245 +653 more	Copy number gain	See cases	GPathogenic
Select item 153441	GRCh38/hg38 2p25.3-22.3(chr2:12770-33711509)x3	LOC126806103, LOC126806104 +1047 more	Copy number gain	See cases	GPathogenic
Select item 152693	GRCh38/hg38 2p25.3-24.1(chr2:17019-20001056)x3	ACP1, ADAM17 +498 more	Copy number gain	See cases	GPathogenic
Select item 148269	GRCh38/hg38 2p25.3-23.3(chr2:17019-26318846)x3	LOC129933186, LOC129933187 +736 more	Copy number gain	See cases	GPathogenic
Select item 146072	GRCh38/hg38 2p25.3-23.2(chr2:30341-28419664)x3	ABHD1, ACP1 +893 more	Copy number gain	See cases	GPathogenic
Select item 59131	GRCh38/hg38 2p25.3-24.3(chr2:30342-14866951)x3	ACP1, ADAM17 +413 more	Copy number gain	See cases	GPathogenic
Select item 59133	GRCh38/hg38 2p25.3-16.1(chr2:66097-55570637)x3	LOC129933311, LOC129933312 +1631 more	Copy number gain	See cases	GPathogenic
Select item 155615	GRCh38/hg38 2p25.3-21(chr2:236816-45983232)x3	LINC01115, LINC01121 +1400 more	Copy number gain	See cases	GPathogenic
Select item 148848	GRCh38/hg38 2p25.3-24.1(chr2:1664615-23664142)x3	ADAM17, ADI1 +546 more	Copy number gain	See cases	GPathogenic
Select item 60105	GRCh38/hg38 2p25.2-24.3(chr2:6531172-16103799)x1	ADAM17, ASAP2 +297 more	Copy number loss	See cases	GPathogenic
Select item 152995	GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3	HAAO, HADHA +2457 more	Copy number gain	See cases	GBenign
Select item 154445	GRCh38/hg38 2p25.1-24.3(chr2:10790663-14417134)x3	C2orf50, E2F6 +98 more	Copy number gain	See cases	GPathogenic
Select item 545241	NC_000002.12:g.(?_11177745)_(16113827_?)del	MYCNUT, NBAS +100 more	Deletion	Schizophrenia	GLikely pathogenic
Select item 2328471	NM_021643.4(TRIB2):c.38G>A (p.Arg13Lys)	TRIB2 (R13K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229006	NM_021643.4(TRIB2):c.56A>G (p.Asn19Ser)	TRIB2 (N19S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182169	NM_021643.4(TRIB2):c.61A>G (p.Thr21Ala)	TRIB2 (T21A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182170	NM_021643.4(TRIB2):c.62C>G (p.Thr21Ser)	TRIB2 (T21S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402739	NM_021643.4(TRIB2):c.76G>C (p.Glu26Gln)	TRIB2 (E26Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275556	NM_021643.4(TRIB2):c.78G>C (p.Glu26Asp)	TRIB2 (E26D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338298	NM_021643.4(TRIB2):c.88A>G (p.Ile30Val)	TRIB2 (I30V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308476	NM_021643.4(TRIB2):c.94T>A (p.Ser32Thr)	TRIB2 (S32T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332840	NM_021643.4(TRIB2):c.179G>C (p.Cys60Ser)	TRIB2 (C60S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182167	NM_021643.4(TRIB2):c.206C>A (p.Pro69His)	TRIB2 (P69H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182168	NM_021643.4(TRIB2):c.230G>A (p.Arg77His)	TRIB2 (R77H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323647	NM_021643.4(TRIB2):c.235G>C (p.Val79Leu)	TRIB2 (V79L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361196	NM_021643.4(TRIB2):c.304G>T (p.Ala102Ser)	TRIB2 (A102S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328607	NM_021643.4(TRIB2):c.326C>A (p.Ala109Asp)	TRIB2 (A109D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328606	NM_021643.4(TRIB2):c.556G>A (p.Glu186Lys)	TRIB2 (E186K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 774809	NM_021643.4(TRIB2):c.563+10A>T	TRIB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3182171	NM_021643.4(TRIB2):c.631G>A (p.Asp211Asn)	TRIB2 (D211N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209272	NM_021643.4(TRIB2):c.655G>A (p.Val219Ile)	TRIB2 (V219I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3182172	NM_021643.4(TRIB2):c.772G>A (p.Glu258Lys)	TRIB2 (E258K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328608	NM_021643.4(TRIB2):c.872G>A (p.Arg291Gln)	TRIB2 (R291Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223913	NM_021643.4(TRIB2):c.940G>A (p.Val314Ile)	TRIB2 (V314I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328605	NM_021643.4(TRIB2):c.955T>C (p.Tyr319His)	TRIB2 (Y319H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3148883	GRCh37/hg19 2p25.3-22.3(chr2:12771-35541353)x3	ABHD1, ACP1 +182 more	Copy number gain	See cases	GPathogenic
Select item 3062616	GRCh37/hg19 2p24.3(chr2:12289529-16104486)x1	DDX1, LRATD1 +4 more	Copy number loss	not specified	GPathogenic
Select item 3062591	GRCh37/hg19 2p25.2-24.1(chr2:6375088-23538518)x3	APOB, ASAP2 +59 more	Copy number gain	not specified	GPathogenic
Select item 1808629	GRCh37/hg19 2p25.3-22.3(chr2:706460-35523639)x3	ABHD1, ADAM17 +177 more	Copy number gain	not provided	GPathogenic
Select item 1708190	GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1	ACTG2, ACTR1B +529 more	Copy number loss	See cases	GPathogenic
Select item 1703543	GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	ABCA12, ABCB11 +1216 more	Copy number gain	Mosaic trisomy 2	GPathogenic
Select item 1340405	GRCh37/hg19 2p25.1-24.3(chr2:8935077-15722794)x1	ADAM17, ASAP2 +29 more	Copy number loss	not provided	GUncertain significance
Select item 814219	GRCh37/hg19 2p25.1-24.3(chr2:11698868-13261503)x3	LPIN1, GREB1 +2 more	Copy number gain	not provided	GUncertain significance
Select item 686578	GRCh37/hg19 2p24.3-24.2(chr2:12269293-18259781)x3	CYRIA, DDX1 +11 more	Copy number gain	not provided	GPathogenic
Select item 443675	GRCh37/hg19 2p25.3-24.1(chr2:12770-20081474)x3	ACP1, ADAM17 +65 more	Copy number gain	See cases	GPathogenic
Select item 442998	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	RGPD4, RGPD5 +1214 more	Copy number gain	See cases	GPathogenic
Select item 442997	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	IL1F10, IL1R1 +1214 more	Copy number gain	See cases	GPathogenic
Select item 442250	GRCh37/hg19 2p24.3(chr2:12677749-14752848)x3	TRIB2	Copy number gain	See cases	GLikely benign

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Items: 48