ClinVar for Gene (Select 5971) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3152895	NM_006509.4(RELB):c.1588G>A (p.Gly530Ser)	RELB (G527S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3152894	NM_006509.4(RELB):c.1430A>G (p.Glu477Gly)	RELB (E474G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3043512	NM_006509.4(RELB):c.1359G>A (p.Pro453=)	RELB	Single nucleotide variant (synonymous variant)	RELB-related disorder	GLikely benign
Select item 3020885	NM_006509.4(RELB):c.663-14C>G	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3019340	NM_006509.4(RELB):c.1080G>A (p.Val360=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3012492	NM_006509.4(RELB):c.1733C>T (p.Ala578Val)	RELB (A575V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3011409	NM_006509.4(RELB):c.505-7C>G	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3007702	NM_006509.4(RELB):c.296C>T (p.Ala99Val)	RELB (A96V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3007296	NM_006509.4(RELB):c.763C>T (p.Leu255=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3007076	NM_006509.4(RELB):c.1188G>A (p.Thr396=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3004949	NM_006509.4(RELB):c.755-3C>T	RELB	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3003573	NM_006509.4(RELB):c.110C>T (p.Ser37Phe)	RELB (S37F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3003516	NM_006509.4(RELB):c.1626G>C (p.Pro542=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2996505	NM_006509.4(RELB):c.324C>T (p.Gly108=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2991836	NM_006509.4(RELB):c.242G>A (p.Arg81His)	RELB (R78H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2991154	NM_006509.4(RELB):c.1231C>T (p.Arg411Trp)	RELB (R408W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2990721	NM_006509.4(RELB):c.325T>A (p.Cys109Ser)	RELB (C109S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2987547	NM_006509.4(RELB):c.1148G>A (p.Arg383Gln)	RELB (R380Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2986295	NM_006509.4(RELB):c.263C>T (p.Ala88Val)	RELB (A85V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2983398	NM_006509.4(RELB):c.840G>C (p.Gln280His)	RELB (Q280H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2981711	NM_006509.4(RELB):c.1116C>G (p.Val372=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2981672	NM_006509.4(RELB):c.844C>T (p.Arg282Cys)	RELB (R282C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2978002	NM_006509.4(RELB):c.1668C>T (p.Asn556=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2974465	NM_006509.4(RELB):c.941C>A (p.Pro314Gln)	RELB (P314Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2969035	NM_006509.4(RELB):c.1635G>A (p.Gly545=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2967292	NM_006509.4(RELB):c.111C>T (p.Ser37=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2966438	NM_006509.4(RELB):c.1548G>A (p.Val516=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2966084	NM_006509.4(RELB):c.1397TCT[1] (p.Phe467del)	RELB (F467del +1 more)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 2962669	NM_006509.4(RELB):c.481A>G (p.Ser161Gly)	RELB (S158G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2961428	NM_006509.4(RELB):c.992-12G>A	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960681	NM_006509.4(RELB):c.201C>G (p.Gly67=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957834	NM_006509.4(RELB):c.140T>C (p.Val47Ala)	RELB (V47A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2906881	NM_006509.4(RELB):c.1440C>T (p.Gly480=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2905397	NM_006509.4(RELB):c.631C>G (p.Arg211Gly)	RELB (R211G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2903606	NM_006509.4(RELB):c.1301G>A (p.Arg434Gln)	RELB (R434Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2902135	NM_006509.4(RELB):c.1114G>A (p.Val372Ile)	RELB (V372I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2898895	NM_006509.4(RELB):c.1588G>C (p.Gly530Arg)	RELB (G527R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2894968	NM_006509.4(RELB):c.1482G>A (p.Thr494=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2893117	NM_006509.4(RELB):c.1370C>T (p.Pro457Leu)	RELB (P454L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2892618	NM_006509.4(RELB):c.638G>A (p.Arg213Gln)	RELB (R213Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2892409	NM_006509.4(RELB):c.755-5G>A	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2889760	NM_006509.4(RELB):c.754G>A (p.Ala252Thr)	RELB (A252T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2888356	NM_006509.4(RELB):c.1605A>G (p.Thr535=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2873071	NM_006509.4(RELB):c.1371G>C (p.Pro457=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2869263	NM_006509.4(RELB):c.662+17C>T	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867889	NM_006509.4(RELB):c.1277-17T>C	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2858353	NM_006509.4(RELB):c.1711C>T (p.Leu571Phe)	RELB (L568F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2857033	NM_006509.4(RELB):c.1097A>G (p.Tyr366Cys)	RELB (Y363C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2854414	NM_006509.4(RELB):c.214C>T (p.Gln72Ter)	RELB (Q69* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2851416	NM_006509.4(RELB):c.886+11A>T	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2849995	NM_006509.4(RELB):c.985C>T (p.Gln329Ter)	RELB (Q326* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2849192	NM_006509.4(RELB):c.1287C>T (p.Gly429=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2847481	NM_006509.4(RELB):c.1582A>T (p.Thr528Ser)	RELB (T528S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2838756	NM_006509.4(RELB):c.465G>T (p.Glu155Asp)	RELB (E152D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2836512	NM_006509.4(RELB):c.886+8G>T	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2835464	NM_006509.4(RELB):c.1181C>T (p.Pro394Leu)	RELB (P391L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2828506	NM_006509.4(RELB):c.1304G>A (p.Arg435Gln)	RELB (R432Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2828023	NM_006509.4(RELB):c.347C>T (p.Ser116Phe)	RELB (S113F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2827752	NM_006509.4(RELB):c.1488C>A (p.Pro496=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2827060	NM_006509.4(RELB):c.421C>T (p.Arg141Cys)	RELB (R138C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2823273	NM_006509.4(RELB):c.795G>A (p.Val265=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2817720	NM_006509.4(RELB):c.107G>A (p.Gly36Glu)	RELB (G36E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2817457	NM_006509.4(RELB):c.1332C>T (p.His444=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2810539	NM_006509.4(RELB):c.685T>C (p.Cys229Arg)	RELB (C226R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2808128	NM_006509.4(RELB):c.645C>A (p.His215Gln)	RELB (H212Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2805344	NM_006509.4(RELB):c.880G>A (p.Asp294Asn)	RELB (D291N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2802895	NM_006509.4(RELB):c.1336C>A (p.Leu446Met)	RELB (L443M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2800673	NM_006509.4(RELB):c.361C>G (p.Pro121Ala)	RELB (P121A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2797227	NM_006509.4(RELB):c.939del (p.Pro314fs)	RELB (P311fs +1 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2796063	NM_006509.4(RELB):c.1722G>A (p.Pro574=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2792272	NM_006509.4(RELB):c.1135G>T (p.Val379Phe)	RELB (V379F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2791271	NM_006509.4(RELB):c.356C>T (p.Pro119Leu)	RELB (P116L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2784380	NM_006509.4(RELB):c.295G>T (p.Ala99Ser)	RELB (A99S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2782736	NM_006509.4(RELB):c.235C>T (p.Leu79=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2780757	NM_006509.4(RELB):c.48G>C (p.Arg16=)	LOC130064661, RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2780441	NM_006509.4(RELB):c.56C>G (p.Pro19Arg)	LOC130064661, RELB (P19R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2780286	NM_006509.4(RELB):c.1567G>A (p.Ala523Thr)	RELB (A520T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2779660	NM_006509.4(RELB):c.991+19C>A	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2778739	NM_006509.4(RELB):c.886+9A>G	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2769635	NM_006509.4(RELB):c.1208-15G>A	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2767651	NM_006509.4(RELB):c.83C>T (p.Ala28Val)	LOC130064661, RELB (A28V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2762878	NM_006509.4(RELB):c.1728T>C (p.Pro576=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2745896	NM_006509.4(RELB):c.1207+17A>G	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2730556	NM_006509.4(RELB):c.337C>G (p.Arg113Gly)	RELB (R113G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2722000	NM_006509.4(RELB):c.1625C>T (p.Pro542Leu)	RELB (P542L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2721672	NM_006509.4(RELB):c.116del (p.Asp39fs)	RELB (D39fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2721405	NM_006509.4(RELB):c.289C>A (p.Pro97Thr)	RELB (P97T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2715922	NM_006509.4(RELB):c.1708G>T (p.Gly570Cys)	RELB (G567C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2714621	NM_006509.4(RELB):c.138C>A (p.Ala46=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2712993	NM_006509.4(RELB):c.976G>A (p.Asp326Asn)	RELB (D323N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2710720	NM_006509.4(RELB):c.991+12G>A	RELB	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2709189	NM_006509.4(RELB):c.505-13T>G	RELB	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2702252	NM_006509.4(RELB):c.847C>T (p.Arg283Trp)	RELB (R280W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2698161	NM_006509.4(RELB):c.1208-3C>A	RELB	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2693267	NM_006509.4(RELB):c.240A>G (p.Pro80=)	RELB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2634981	NM_006509.4(RELB):c.1216G>A (p.Gly406Ser)	RELB (G403S +1 more)	Single nucleotide variant (missense variant)	RELB-related disorder +1 more	GUncertain significance
Select item 2628130	NM_006509.4(RELB):c.755-65T>C	RELB	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2628126	NM_006509.4(RELB):c.1207+29C>G	RELB	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2612129	NM_006509.4(RELB):c.859G>A (p.Val287Met)	RELB (V287M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560946	NM_006509.4(RELB):c.1327G>A (p.Asp443Asn)	RELB (D440N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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