"PreventionGenetics, part of Exact Sciences"[submitter] AND "REST"[gen - ClinVar

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Items: 53

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2629540	NM_005612.5(REST):c.68G>A (p.Gly23Glu)	REST (G23E)	Single nucleotide variant (missense variant)	REST-related condition +2 more	GUncertain significance
Select item 3033506	NM_005612.5(REST):c.131C>G (p.Pro44Arg)	REST (P44R)	Single nucleotide variant (missense variant)	REST-related condition	GUncertain significance
Select item 1152352	NM_005612.5(REST):c.183CTG[1] (p.Cys63del)	REST (C63del)	Microsatellite (inframe_deletion)	REST-related condition +1 more	GLikely benign
Select item 714280	NM_005612.5(REST):c.274G>A (p.Gly92Arg)	REST (G92R)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GBenign/Likely benign
Select item 1130157	NM_005612.5(REST):c.324C>T (p.Asn108=)	REST	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1637814	NM_005612.5(REST):c.336A>G (p.Arg112=)	REST	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 712906	NM_005612.5(REST):c.367C>G (p.Pro123Ala)	REST (P123A)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GBenign/Likely benign
Select item 2628435	NM_005612.5(REST):c.380C>T (p.Ala127Val)	REST (A127V)	Single nucleotide variant (missense variant)	REST-related condition	GUncertain significance
Select item 847313	NM_005612.5(REST):c.422C>G (p.Pro141Arg)	REST (P141R)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1589591	NM_005612.5(REST):c.459C>T (p.Ser153=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition +1 more	GLikely benign
Select item 2631409	NM_005612.5(REST):c.533T>A (p.Ile178Asn)	REST (I178N)	Single nucleotide variant (missense variant)	REST-related condition	GUncertain significance
Select item 1428170	NM_005612.5(REST):c.614C>T (p.Thr205Ile)	REST (T205I)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GUncertain significance
Select item 714477	NM_005612.5(REST):c.618A>C (p.Ala206=)	REST	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1309829	NM_005612.5(REST):c.645dup (p.Ile216fs)	REST (I216fs)	Duplication (frameshift variant)	not provided +1 more	GUncertain significance
Select item 2632513	NM_005612.5(REST):c.764del (p.Tyr255fs)	REST (Y255fs)	Deletion (frameshift variant)	REST-related condition	GLikely pathogenic
Select item 2633455	NM_005612.5(REST):c.843C>G (p.Cys281Trp)	REST (C281W)	Single nucleotide variant (missense variant)	REST-related condition	GUncertain significance
Select item 2635523	NM_005612.5(REST):c.908del (p.Pro303fs)	REST (P303fs)	Deletion (frameshift variant)	REST-related condition	GLikely pathogenic
Select item 1265482	NM_005612.5(REST):c.983-2256G>A	REST	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 3030152	NM_005612.5(REST):c.983-2245A>G	REST	Single nucleotide variant (intron variant)	REST-related condition	GLikely benign
Select item 1168380	NM_005612.5(REST):c.1095C>T (p.His365=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition +1 more	GBenign/Likely benign
Select item 3044985	NM_005612.5(REST):c.1170T>A (p.Asn390Lys)	REST (N390K)	Single nucleotide variant (missense variant)	REST-related condition	GUncertain significance
Select item 1143239	NM_005612.5(REST):c.1279C>T (p.Leu427=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition +1 more	GLikely benign
Select item 1014552	NM_005612.5(REST):c.1343T>C (p.Ile448Thr)	REST (I448T)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GUncertain significance
Select item 3056774	NM_005612.5(REST):c.1374T>C (p.Ala458=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition	GLikely benign
Select item 722055	NM_005612.5(REST):c.1453G>A (p.Val485Met)	REST (V485M)	Single nucleotide variant (missense variant)	REST-related condition +2 more	GLikely benign
Select item 2035957	NM_005612.5(REST):c.1458C>T (p.Ile486=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition +1 more	GLikely benign
Select item 1008098	NM_005612.5(REST):c.1640T>C (p.Val547Ala)	REST (V547A)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GLikely benign
Select item 1591842	NM_005612.5(REST):c.1706A>T (p.Lys569Ile)	REST (K569I)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GLikely benign
Select item 2885711	NM_005612.5(REST):c.1869G>A (p.Lys623=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition +1 more	GLikely benign
Select item 1166071	NM_005612.5(REST):c.1875C>T (p.Pro625=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition +1 more	GBenign/Likely benign
Select item 1135056	NM_005612.5(REST):c.1902G>A (p.Met634Ile)	REST (M634I)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 714478	NM_005612.5(REST):c.2008G>A (p.Val670Met)	REST (V670M)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3036135	NM_005612.5(REST):c.2088G>A (p.Thr696=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition	GLikely benign
Select item 3061089	NM_005612.5(REST):c.2115C>G (p.Pro705=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition	GLikely benign
Select item 2635000	NM_005612.5(REST):c.2164_2211del (p.Gln722_Met737del)	REST	Deletion (inframe_deletion)	not provided +1 more	GUncertain significance
Select item 769634	NM_005612.5(REST):c.2206C>T (p.Pro736Ser)	REST (P736S)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GBenign/Likely benign
Select item 1165025	NM_005612.5(REST):c.2236C>A (p.Gln746Lys)	REST (Q746K)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GBenign/Likely benign
Select item 745625	NM_005612.5(REST):c.2248T>A (p.Ser750Thr)	REST (S750T)	Single nucleotide variant (missense variant)	REST-related condition +2 more	GConflicting classifications of pathogenicity
Select item 1089088	NM_005612.5(REST):c.2287A>G (p.Ile763Val)	REST (I763V)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GLikely benign
Select item 3031292	NM_005612.5(REST):c.2340G>A (p.Glu780=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition	GLikely benign
Select item 1353310	NM_005612.5(REST):c.2354T>C (p.Met785Thr)	REST (M785T)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GUncertain significance
Select item 2631457	NM_005612.5(REST):c.2374C>T (p.Pro792Ser)	REST (P792S)	Single nucleotide variant (missense variant)	REST-related condition	GUncertain significance
Select item 1050137	NM_005612.5(REST):c.2443C>T (p.Pro815Ser)	REST (P815S)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GBenign/Likely benign
Select item 850478	NM_005612.5(REST):c.2486A>G (p.Glu829Gly)	REST (E829G)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3060915	NM_005612.5(REST):c.2532T>C (p.Pro844=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition	GLikely benign
Select item 1092831	NM_005612.5(REST):c.2541T>C (p.Asp847=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition +1 more	GLikely benign
Select item 710927	NM_005612.5(REST):c.2557G>C (p.Glu853Gln)	REST (E853Q)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GBenign
Select item 1126680	NM_005612.5(REST):c.2778G>A (p.Leu926=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition +1 more	GLikely benign
Select item 2631848	NM_005612.5(REST):c.2945G>A (p.Arg982His)	REST (R982H)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GUncertain significance
Select item 1169920	NM_005612.5(REST):c.3120A>G (p.Gln1040=)	REST	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 961509	NM_005612.5(REST):c.3164C>T (p.Ala1055Val)	REST (A1055V)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3044943	NM_005612.5(REST):c.3234C>T (p.His1078=)	REST	Single nucleotide variant (synonymous variant)	REST-related condition	GLikely benign
Select item 2178538	NM_005612.5(REST):c.3239A>G (p.Asn1080Ser)	REST (N1080S)	Single nucleotide variant (missense variant)	REST-related condition +1 more	GUncertain significance

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Items: 53