ClinVar for Gene (Select 23650) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3461250	NM_012101.4(TRIM29):c.942C>A (p.Phe314Leu)	TRIM29 (F53L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3461249	NM_012101.4(TRIM29):c.1475G>C (p.Arg492Pro)	TRIM29 (R231P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3461248	NM_012101.4(TRIM29):c.1604G>A (p.Gly535Asp)	TRIM29 (G274D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3461247	NM_012101.4(TRIM29):c.893G>A (p.Arg298His)	TRIM29 (R37H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3461246	NM_012101.4(TRIM29):c.1004G>A (p.Arg335Gln)	TRIM29 (R335Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3461245	NM_012101.4(TRIM29):c.1265G>T (p.Arg422Leu)	LOC112042780, TRIM29 (R161L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3461244	NM_012101.4(TRIM29):c.1364C>T (p.Thr455Met)	TRIM29 (T455M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3461242	NM_012101.4(TRIM29):c.1265G>A (p.Arg422His)	LOC112042780, TRIM29 (R161H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328693	NM_012101.4(TRIM29):c.1154G>C (p.Ser385Thr)	TRIM29 (S124T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328692	NM_012101.4(TRIM29):c.254C>A (p.Ser85Tyr)	TRIM29 (S85Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328691	NM_012101.4(TRIM29):c.1074T>A (p.His358Gln)	TRIM29 (H358Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328690	NM_012101.4(TRIM29):c.1243G>A (p.Asp415Asn)	LOC112042780, TRIM29 (D415N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328688	NM_012101.4(TRIM29):c.553A>G (p.Lys185Glu)	TRIM29 (K185E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328687	NM_012101.4(TRIM29):c.1099C>A (p.Leu367Met)	TRIM29 (L367M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328686	NM_012101.4(TRIM29):c.1163C>G (p.Ser388Cys)	TRIM29 (S388C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182357	NM_012101.4(TRIM29):c.859G>T (p.Asp287Tyr)	TRIM29 (D26Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182356	NM_012101.4(TRIM29):c.776C>T (p.Thr259Ile)	TRIM29 (T259I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182355	NM_012101.4(TRIM29):c.762T>A (p.Asn254Lys)	TRIM29 (N254K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182353	NM_012101.4(TRIM29):c.319G>C (p.Ala107Pro)	TRIM29 (A107P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182352	NM_012101.4(TRIM29):c.311C>T (p.Ser104Leu)	TRIM29 (S104L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182351	NM_012101.4(TRIM29):c.259G>A (p.Asp87Asn)	TRIM29 (D87N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182350	NM_012101.4(TRIM29):c.219T>A (p.Asn73Lys)	TRIM29 (N73K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182349	NM_012101.4(TRIM29):c.1759G>A (p.Ala587Thr)	TRIM29 (A326T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182348	NM_012101.4(TRIM29):c.1750T>G (p.Ser584Ala)	TRIM29 (S584A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182347	NM_012101.4(TRIM29):c.1708C>G (p.His570Asp)	TRIM29 (H570D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182346	NM_012101.4(TRIM29):c.1694A>G (p.Gln565Arg)	TRIM29 (Q565R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182345	NM_012101.4(TRIM29):c.1610C>G (p.Ser537Cys)	TRIM29 (S276C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182344	NM_012101.4(TRIM29):c.151G>C (p.Ala51Pro)	TRIM29 (A51P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182343	NM_012101.4(TRIM29):c.1508A>G (p.Asn503Ser)	TRIM29 (N242S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182341	NM_012101.4(TRIM29):c.1394C>T (p.Pro465Leu)	TRIM29 (P204L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182339	NM_012101.4(TRIM29):c.1006G>A (p.Glu336Lys)	TRIM29 (E75K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3148862	GRCh37/hg19 11q23.3-25(chr11:116683755-134937416)x3	ABCG4, ACAD8 +177 more	Copy number gain	not provided	GPathogenic
Select item 2684657	GRCh37/hg19 11q23.3-24.1(chr11:119688645-122861792)x3	ARHGEF12, BLID +16 more	Copy number gain	not provided	GUncertain significance
Select item 2671625	Single allele	AASDHPPT, ABCG4 +275 more	Duplication	not provided	GPathogenic
Select item 2618042	NM_012101.4(TRIM29):c.955C>T (p.Arg319Trp)	TRIM29 (R319W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608625	NM_012101.4(TRIM29):c.830A>C (p.Gln277Pro)	TRIM29 (Q16P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592728	NM_012101.4(TRIM29):c.1172C>A (p.Pro391Gln)	TRIM29 (P130Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548574	NM_012101.4(TRIM29):c.864A>C (p.Glu288Asp)	TRIM29 (E288D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541955	NM_012101.4(TRIM29):c.1373T>G (p.Phe458Cys)	TRIM29 (F458C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540452	NM_012101.4(TRIM29):c.404C>A (p.Ser135Tyr)	TRIM29 (S135Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533244	NM_012101.4(TRIM29):c.1495C>G (p.Gln499Glu)	TRIM29 (Q499E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524557	NM_012101.4(TRIM29):c.1601A>G (p.Gln534Arg)	TRIM29 (Q273R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517287	NM_012101.4(TRIM29):c.432G>T (p.Glu144Asp)	TRIM29 (E144D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507723	NM_012101.4(TRIM29):c.1172C>T (p.Pro391Leu)	TRIM29 (P130L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487188	NM_012101.4(TRIM29):c.1021G>A (p.Asp341Asn)	TRIM29 (D80N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484157	NM_012101.4(TRIM29):c.1334G>A (p.Gly445Asp)	TRIM29 (G184D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458198	NM_012101.4(TRIM29):c.1264C>T (p.Arg422Cys)	LOC112042780, TRIM29 (R161C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455774	NM_012101.4(TRIM29):c.88G>A (p.Glu30Lys)	TRIM29 (E30K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2425350	NC_000011.9:g.(?_119103138)_(121060609_?)dup	ARHGEF12, C1QTNF5 +14 more	Duplication	not provided	GUncertain significance
Select item 2422557	NC_000011.9:g.(?_117209303)_(120133495_?)dup	ABCG4, ARCN1 +54 more	Duplication	not provided	GUncertain significance
Select item 2422303	NC_000011.9:g.(?_116691583)_(121500272_?)dup	ABCG4, APOA1 +72 more	Duplication	RASopathy +5 more	GUncertain significance
Select item 2400747	NM_012101.4(TRIM29):c.1229G>A (p.Gly410Asp)	LOC112042780, TRIM29 (G149D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392113	NM_012101.4(TRIM29):c.1544G>A (p.Arg515Gln)	TRIM29 (R254Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362959	NM_012101.4(TRIM29):c.1300C>T (p.Arg434Cys)	LOC112042780, TRIM29 (R173C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356620	NM_012101.4(TRIM29):c.537C>G (p.Asn179Lys)	TRIM29 (N179K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353737	NM_012101.4(TRIM29):c.1289C>T (p.Ala430Val)	LOC112042780, TRIM29 (A169V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341630	NM_012101.4(TRIM29):c.1172C>G (p.Pro391Arg)	TRIM29 (P391R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341580	NM_012101.4(TRIM29):c.463C>T (p.Arg155Trp)	TRIM29 (R155W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338769	NM_012101.4(TRIM29):c.1504T>G (p.Phe502Val)	TRIM29 (F502V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316787	NM_012101.4(TRIM29):c.1102C>G (p.His368Asp)	TRIM29 (H368D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294321	NM_012101.4(TRIM29):c.1281G>A (p.Met427Ile)	LOC112042780, TRIM29 (M166I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279889	NM_012101.4(TRIM29):c.1301G>C (p.Arg434Pro)	LOC112042780, TRIM29 (R173P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271562	NM_012101.4(TRIM29):c.1463C>T (p.Ser488Leu)	TRIM29 (S488L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263541	NM_012101.4(TRIM29):c.1403T>C (p.Met468Thr)	TRIM29 (M207T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256197	NM_012101.4(TRIM29):c.296T>C (p.Met99Thr)	TRIM29 (M99T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255613	NM_012101.4(TRIM29):c.17C>T (p.Ala6Val)	TRIM29 (A6V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250977	NM_012101.4(TRIM29):c.668G>A (p.Arg223His)	TRIM29 (R223H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246577	NM_012101.4(TRIM29):c.1270G>A (p.Val424Ile)	LOC112042780, TRIM29 (V424I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243182	NM_012101.4(TRIM29):c.1741G>A (p.Gly581Arg)	TRIM29 (G320R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240628	NM_012101.4(TRIM29):c.772G>T (p.Val258Leu)	TRIM29 (V258L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228884	NM_012101.4(TRIM29):c.1204G>T (p.Gly402Trp)	TRIM29 (G402W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220137	NM_012101.4(TRIM29):c.892C>T (p.Arg298Cys)	TRIM29 (R37C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217862	NM_012101.4(TRIM29):c.942C>G (p.Phe314Leu)	TRIM29 (F53L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216541	NM_012101.4(TRIM29):c.1340A>C (p.Asp447Ala)	TRIM29 (D186A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212355	NM_012101.4(TRIM29):c.806C>T (p.Thr269Met)	TRIM29 (T269M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204942	NM_012101.4(TRIM29):c.1003C>T (p.Arg335Trp)	TRIM29 (R74W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1704646	GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3	MAML2, MAP3K11 +955 more	Copy number gain	MISSED ABORTION	GPathogenic
Select item 1410294	NC_000011.9:g.(?_116660844)_(121500272_?)dup	RNF26, TAGLN +73 more	Duplication	not provided	GUncertain significance
Select item 1341168	GRCh37/hg19 11q23.1-24.3(chr11:112375478-128785742)x3	ABCG4, ACRV1 +172 more	Copy number gain	not provided	GPathogenic
Select item 1015400	NC_000011.9:g.(?_119077108)_(120133495_?)dup	C1QTNF5, CBL +9 more	Duplication	RASopathy	GUncertain significance
Select item 973579	NC_000011.9:g.104288964_134937416dup	VSIG2, VWA5A +259 more	Duplication	Distal trisomy 11q	GPathogenic
Select item 812956	Single allele	APLP2, LINC02873 +169 more	Deletion	Anemia +7 more	GLikely pathogenic
Select item 781049	NM_012101.4(TRIM29):c.1333+8C>A	LOC112042780, TRIM29	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 710126	NM_012101.4(TRIM29):c.642C>G (p.Leu214=)	TRIM29	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 687452	GRCh37/hg19 11q23.3-25(chr11:117830263-134938470)x3	CD3G, CDON +160 more	Copy number gain	not provided	GPathogenic
Select item 625808	GRCh37/hg19 11q23.3-25(chr11:116700253-134904063)	BACE1, BACE1-AS +176 more	Copy number gain	not provided	GPathogenic
Select item 625659	GRCh37/hg19 11q23.3-25(chr11:116691675-134889485)	ARHGAP32, ARHGEF12 +177 more	Copy number gain	not provided	GPathogenic
Select item 563884	GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3	ABCG4, ACAD8 +177 more	Copy number gain	not provided	GPathogenic
Select item 563882	GRCh37/hg19 11q23.3-25(chr11:119538664-134938470)x1	ACAD8, ACRV1 +114 more	Copy number loss	not provided	GPathogenic
Select item 563876	GRCh37/hg19 11q23.3(chr11:116669751-120979377)x3	ABCG4, APOA1 +70 more	Copy number gain	not provided	GLikely pathogenic
Select item 545140	Single allele	ABCG4, ACAD8 +608 more	Duplication	Schizophrenia	GLikely pathogenic
Select item 441904	GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)	AAMDC, AASDHPPT +1289 more	Copy number gain	See cases	GPathogenic
Select item 441903	GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3	SLC37A4, SNORD26 +1289 more	Copy number gain	See cases	GPathogenic
Select item 441664	GRCh37/hg19 11q23.3-25(chr11:116681007-134938470)x3	ABCG4, ACAD8 +177 more	Copy number gain	See cases	GPathogenic
Select item 253601	GRCh37/hg19 11q23.3-25(chr11:119807473-134868407)x1	ACAD8, ACRV1 +113 more	Copy number loss	See cases	GPathogenic
Select item 253520	GRCh37/hg19 11q23.3(chr11:115215434-120559928)x3	ABCG4, APOA1 +72 more	Copy number gain	See cases	GPathogenic
Select item 161071	GRCh38/hg38 11q23.3-25(chr11:116851395-134998513)x3	ABCG4, ACAD8 +764 more	Copy number gain	See cases	GPathogenic
Select item 151354	GRCh38/hg38 11q23.3-24.2(chr11:120080142-125829106)x1	ACRV1, ARHGEF12 +255 more	Copy number loss	See cases	GPathogenic
Select item 150522	GRCh38/hg38 11q23.3-24.2(chr11:117333952-127709156)x3	LOC130007002, LOC130007003 +499 more	Copy number gain	See cases	GPathogenic
Select item 150032	GRCh38/hg38 11q23.3-25(chr11:119424297-135075271)x1	LOC130006995, LOC130006996 +551 more	Copy number loss	See cases	GPathogenic

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