ClinVar for Gene (Select 254048) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3465244	NM_173569.4(UBN2):c.2645A>G (p.Gln882Arg)	UBN2 (Q882R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465243	NM_173569.4(UBN2):c.176C>A (p.Pro59His)	LOC129999464, UBN2 (P59H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465242	NM_173569.4(UBN2):c.3718A>G (p.Met1240Val)	UBN2 (M1240V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465241	NM_173569.4(UBN2):c.3483C>A (p.Asn1161Lys)	UBN2 (N1161K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465240	NM_173569.4(UBN2):c.3475G>A (p.Gly1159Arg)	UBN2 (G1159R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465239	NM_173569.4(UBN2):c.718A>G (p.Asn240Asp)	UBN2 (N240D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465238	NM_173569.4(UBN2):c.110G>A (p.Arg37Gln)	LOC129999464, UBN2 (R37Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465237	NM_173569.4(UBN2):c.3875C>G (p.Ala1292Gly)	UBN2 (A1292G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465236	NM_173569.4(UBN2):c.1765G>T (p.Asp589Tyr)	UBN2 (D589Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465235	NM_173569.4(UBN2):c.2011C>G (p.Leu671Val)	UBN2 (L671V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465233	NM_173569.4(UBN2):c.854A>G (p.Glu285Gly)	UBN2 (E285G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465232	NM_173569.4(UBN2):c.563G>T (p.Gly188Val)	UBN2 (G188V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465231	NM_173569.4(UBN2):c.3574A>G (p.Thr1192Ala)	UBN2 (T1192A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465230	NM_173569.4(UBN2):c.3886C>T (p.His1296Tyr)	UBN2 (H1296Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465229	NM_173569.4(UBN2):c.290C>T (p.Pro97Leu)	LOC129999464, UBN2 (P97L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465228	NM_173569.4(UBN2):c.341C>T (p.Ser114Phe)	UBN2 (S114F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465227	NM_173569.4(UBN2):c.3100G>A (p.Ala1034Thr)	UBN2 (A1034T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465226	NM_173569.4(UBN2):c.3064A>T (p.Ile1022Phe)	UBN2 (I1022F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465225	NM_173569.4(UBN2):c.23C>T (p.Ala8Val)	UBN2 (A8V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465224	NM_173569.4(UBN2):c.2077G>A (p.Val693Ile)	UBN2 (V693I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465222	NM_173569.4(UBN2):c.2249T>C (p.Ile750Thr)	UBN2 (I750T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465221	NM_173569.4(UBN2):c.2392C>T (p.Arg798Cys)	UBN2 (R798C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3465220	NM_173569.4(UBN2):c.3887A>G (p.His1296Arg)	UBN2 (H1296R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3392069	GRCh37/hg19 7q33-34(chr7:137682885-140654909)x3	ADCK2, AKR1D1 +24 more	Copy number gain	not provided	GUncertain significance
Select item 3391898	GRCh37/hg19 7q33-36.1(chr7:136304444-148292957)x1	ADCK2, AGK +87 more	Copy number loss	not provided	GPathogenic
Select item 3391897	GRCh37/hg19 7q31.32-36.1(chr7:122190535-149944340)x1	ACTR3C, ADCK2 +199 more	Copy number loss	not provided	GPathogenic
Select item 3345492	NM_173569.4(UBN2):c.1976T>G (p.Met659Arg)	UBN2 (M659R)	Single nucleotide variant (missense variant)	UBN2-related disorder	GUncertain significance
Select item 3344553	NM_173569.4(UBN2):c.1791A>G (p.Ile597Met)	UBN2 (I597M)	Single nucleotide variant (missense variant)	UBN2-related disorder	GUncertain significance
Select item 3330648	NM_173569.4(UBN2):c.2450C>T (p.Thr817Ile)	UBN2 (T817I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330647	NM_173569.4(UBN2):c.1589A>G (p.Asn530Ser)	UBN2 (N530S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330645	NM_173569.4(UBN2):c.2506C>G (p.His836Asp)	UBN2 (H836D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330644	NM_173569.4(UBN2):c.176C>T (p.Pro59Leu)	LOC129999464, UBN2 (P59L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330643	NM_173569.4(UBN2):c.1019A>G (p.Lys340Arg)	UBN2 (K340R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330642	NM_173569.4(UBN2):c.3448A>G (p.Thr1150Ala)	UBN2 (T1150A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330641	NM_173569.4(UBN2):c.503A>G (p.Asp168Gly)	UBN2 (D168G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330640	NM_173569.4(UBN2):c.2936T>C (p.Met979Thr)	UBN2 (M979T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330639	NM_173569.4(UBN2):c.1511G>C (p.Gly504Ala)	UBN2 (G504A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3330638	NM_173569.4(UBN2):c.3047A>G (p.Lys1016Arg)	UBN2 (K1016R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185700	NM_173569.4(UBN2):c.845A>C (p.Lys282Thr)	UBN2 (K282T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185699	NM_173569.4(UBN2):c.827T>C (p.Ile276Thr)	UBN2 (I276T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185698	NM_173569.4(UBN2):c.765T>A (p.Asp255Glu)	UBN2 (D255E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3185697	NM_173569.4(UBN2):c.752A>T (p.Asp251Val)	UBN2 (D251V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185696	NM_173569.4(UBN2):c.751G>T (p.Asp251Tyr)	UBN2 (D251Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185695	NM_173569.4(UBN2):c.406C>G (p.Pro136Ala)	UBN2 (P136A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185694	NM_173569.4(UBN2):c.4027C>A (p.Pro1343Thr)	UBN2 (P1343T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185693	NM_173569.4(UBN2):c.344G>A (p.Arg115Gln)	UBN2 (R115Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185692	NM_173569.4(UBN2):c.343C>G (p.Arg115Gly)	UBN2 (R115G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185691	NM_173569.4(UBN2):c.3154C>A (p.Leu1052Met)	UBN2 (L1052M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185690	NM_173569.4(UBN2):c.3071C>T (p.Thr1024Met)	UBN2 (T1024M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185689	NM_173569.4(UBN2):c.3052A>G (p.Met1018Val)	UBN2 (M1018V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185688	NM_173569.4(UBN2):c.2912T>C (p.Ile971Thr)	UBN2 (I971T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185686	NM_173569.4(UBN2):c.2648G>A (p.Arg883Lys)	UBN2 (R883K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185685	NM_173569.4(UBN2):c.2542G>T (p.Ala848Ser)	UBN2 (A848S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185684	NM_173569.4(UBN2):c.2470A>T (p.Thr824Ser)	UBN2 (T824S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185683	NM_173569.4(UBN2):c.236G>A (p.Arg79His)	LOC129999464, UBN2 (R79H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185682	NM_173569.4(UBN2):c.233G>A (p.Ser78Asn)	LOC129999464, UBN2 (S78N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185681	NM_173569.4(UBN2):c.2258A>G (p.Asp753Gly)	UBN2 (D753G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185680	NM_173569.4(UBN2):c.2243A>C (p.Glu748Ala)	UBN2 (E748A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185679	NM_173569.4(UBN2):c.1309A>C (p.Thr437Pro)	UBN2 (T437P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185678	NM_173569.4(UBN2):c.124C>T (p.Pro42Ser)	LOC129999464, UBN2 (P42S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062984	GRCh37/hg19 7q33-36.3(chr7:137456457-159119707)x3	ABCB8, ABCF2 +165 more	Copy number gain	not specified	GPathogenic
Select item 3058609	NM_173569.4(UBN2):c.3153C>T (p.Pro1051=)	UBN2	Single nucleotide variant (synonymous variant)	UBN2-related disorder	GLikely benign
Select item 3057481	NM_173569.4(UBN2):c.2511A>G (p.Thr837=)	UBN2	Single nucleotide variant (synonymous variant)	UBN2-related disorder	GLikely benign
Select item 3055692	NM_173569.4(UBN2):c.3000T>G (p.Val1000=)	UBN2	Single nucleotide variant (synonymous variant)	UBN2-related disorder	GLikely benign
Select item 3055511	NM_173569.4(UBN2):c.3162G>A (p.Ser1054=)	UBN2	Single nucleotide variant (synonymous variant)	UBN2-related disorder	GBenign
Select item 3053845	NM_173569.4(UBN2):c.385C>T (p.Leu129=)	UBN2	Single nucleotide variant (synonymous variant)	UBN2-related disorder	GLikely benign
Select item 3053038	NM_173569.4(UBN2):c.906-10G>A	UBN2	Single nucleotide variant (intron variant)	UBN2-related disorder	GLikely benign
Select item 3050098	NM_173569.4(UBN2):c.1694G>A (p.Arg565His)	UBN2 (R565H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3049290	NM_173569.4(UBN2):c.2471C>T (p.Thr824Ile)	UBN2 (T824I)	Single nucleotide variant (missense variant)	UBN2-related disorder	GBenign
Select item 3044425	NM_173569.4(UBN2):c.1462C>T (p.Leu488=)	UBN2	Single nucleotide variant (synonymous variant)	UBN2-related disorder	GLikely benign
Select item 3039631	NM_173569.4(UBN2):c.905+5G>A	UBN2	Single nucleotide variant (intron variant)	UBN2-related disorder	GBenign
Select item 3034071	NM_173569.4(UBN2):c.2937G>A (p.Met979Ile)	UBN2 (M979I)	Single nucleotide variant (missense variant)	UBN2-related disorder	GLikely benign
Select item 3033481	NM_173569.4(UBN2):c.358C>T (p.Pro120Ser)	UBN2 (P120S)	Single nucleotide variant (missense variant)	UBN2-related disorder	GBenign
Select item 2690407	NM_173569.4(UBN2):c.3781G>T (p.Val1261Phe)	UBN2 (V1261F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2685271	GRCh37/hg19 7q33-36.3(chr7:135639005-159119707)x1	ARHGEF35, KEL +169 more	Copy number loss	not provided	GPathogenic
Select item 2681632	NM_173569.4(UBN2):c.2530C>T (p.Pro844Ser)	UBN2 (P844S)	Single nucleotide variant (missense variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2658014	NM_173569.4(UBN2):c.222G>A (p.Gln74=)	LOC129999464, UBN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2637049	NM_173569.4(UBN2):c.3979C>T (p.Gln1327Ter)	UBN2 (Q1327*)	Single nucleotide variant (nonsense)	UBN2-related disorder	GUncertain significance
Select item 2633884	NM_173569.4(UBN2):c.3706C>T (p.Pro1236Ser)	UBN2 (P1236S)	Single nucleotide variant (missense variant)	UBN2-related disorder	GUncertain significance
Select item 2632864	NM_173569.4(UBN2):c.1140C>A (p.Asp380Glu)	UBN2 (D380E)	Single nucleotide variant (missense variant)	UBN2-related disorder	GUncertain significance
Select item 2631094	NM_173569.4(UBN2):c.1993C>T (p.Arg665Trp)	UBN2 (R665W)	Single nucleotide variant (missense variant)	UBN2-related disorder	GUncertain significance
Select item 2621401	NM_173569.4(UBN2):c.950G>A (p.Arg317His)	UBN2 (R317H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613935	NM_173569.4(UBN2):c.3169C>T (p.Pro1057Ser)	UBN2 (P1057S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597867	NM_173569.4(UBN2):c.2878A>G (p.Asn960Asp)	UBN2 (N960D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2579171	GRCh38/hg38 7q34-36.3(chr7:138620939-159233475)x3	LOC129999716, LOC129999717 +847 more	Copy number gain	Neurodevelopmental disorder	GLikely pathogenic
Select item 2579170	GRCh38/hg38 7q33-36.3(chr7:137463392-159345973)x3	EPHA1-AS1, EPHB6 +888 more	Copy number gain	Neurodevelopmental disorder	GPathogenic
Select item 2569846	NM_173569.4(UBN2):c.2942G>A (p.Arg981His)	UBN2 (R981H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549184	NM_173569.4(UBN2):c.3649G>C (p.Val1217Leu)	UBN2 (V1217L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548576	NM_173569.4(UBN2):c.677T>C (p.Val226Ala)	UBN2 (V226A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548499	NM_173569.4(UBN2):c.3121G>T (p.Ala1041Ser)	UBN2 (A1041S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544239	NM_173569.4(UBN2):c.1643G>A (p.Ser548Asn)	UBN2 (S548N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540627	NM_173569.4(UBN2):c.2884C>T (p.Pro962Ser)	UBN2 (P962S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540453	NM_173569.4(UBN2):c.1034A>G (p.Lys345Arg)	UBN2 (K345R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537901	NM_173569.4(UBN2):c.3068C>T (p.Ser1023Phe)	UBN2 (S1023F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531428	NM_173569.4(UBN2):c.1148T>C (p.Ile383Thr)	UBN2 (I383T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529170	NM_173569.4(UBN2):c.3239A>C (p.Asn1080Thr)	UBN2 (N1080T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524328	NM_173569.4(UBN2):c.3121G>A (p.Ala1041Thr)	UBN2 (A1041T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494471	NM_173569.4(UBN2):c.104C>A (p.Pro35His)	LOC129999464, UBN2 (P35H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489758	NM_173569.4(UBN2):c.3242C>G (p.Pro1081Arg)	UBN2 (P1081R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461127	NM_173569.4(UBN2):c.1078T>C (p.Cys360Arg)	UBN2 (C360R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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