"Ambry Genetics"[submitter] AND "PER3"[gene] - ClinVar

Search results

Items: 87

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2350209	NM_001377275.1(PER3):c.35G>T (p.Arg12Leu)	PER3 (R12L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530523	NM_001377275.1(PER3):c.93C>A (p.Phe31Leu)	PER3 (F31L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305813	NM_001377275.1(PER3):c.103A>G (p.Arg35Gly)	PER3 (R35G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292250	NM_001377275.1(PER3):c.198C>G (p.Phe66Leu)	PER3 (F66L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314743	NM_001377275.1(PER3):c.203C>T (p.Ser68Leu)	PER3 (S68L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239303	NM_001377275.1(PER3):c.232G>C (p.Asp78His)	PER3 (D78H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407380	NM_001377275.1(PER3):c.242A>G (p.Asn81Ser)	PER3 (N81S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590017	NM_001377275.1(PER3):c.253C>T (p.Arg85Cys)	PER3 (R85C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3211456	NM_001377275.1(PER3):c.361A>G (p.Ile121Val)	PER3 (I121V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513220	NM_001377275.1(PER3):c.364G>A (p.Ala122Thr)	PER3 (A122T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3211457	NM_001377275.1(PER3):c.439A>G (p.Ile147Val)	PER3 (I147V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2605613	NM_001377275.1(PER3):c.455C>T (p.Ala152Val)	PER3 (A152V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 252710	NM_001377275.1(PER3):c.470G>A (p.Arg157His)	PER3 (R157H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3211458	NM_001377275.1(PER3):c.488C>T (p.Ala163Val)	PER3 (A163V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305811	NM_001377275.1(PER3):c.539A>G (p.Tyr180Cys)	PER3 (Y180C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3305807	NM_001377275.1(PER3):c.541G>A (p.Ala181Thr)	PER3 (A181T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3211459	NM_001377275.1(PER3):c.542C>T (p.Ala181Val)	PER3 (A181V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238006	NM_001377275.1(PER3):c.605A>C (p.Tyr202Ser)	PER3 (Y201S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3211460	NM_001377275.1(PER3):c.620T>G (p.Val207Gly)	PER3 (V207G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3211461	NM_001377275.1(PER3):c.682C>G (p.Pro228Ala)	PER3 (P227A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460980	NM_001377275.1(PER3):c.697C>G (p.Pro233Ala)	PER3 (P232A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284008	NM_001377275.1(PER3):c.757C>G (p.Leu253Val)	PER3 (L252V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488158	NM_001377275.1(PER3):c.796C>T (p.Pro266Ser)	PER3 (P265S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3211462	NM_001377275.1(PER3):c.806C>T (p.Pro269Leu)	PER3 (P269L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546786	NM_001377275.1(PER3):c.899C>T (p.Pro300Leu)	PER3 (P300L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320357	NM_001377275.1(PER3):c.1051A>G (p.Ile351Val)	PER3 (I351V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3211449	NM_001377275.1(PER3):c.1120C>T (p.Arg374Trp)	PER3 (R373W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324677	NM_001377275.1(PER3):c.1153G>A (p.Asp385Asn)	PER3 (D385N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305810	NM_001377275.1(PER3):c.1232T>C (p.Leu411Pro)	PER3 (L410P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305815	NM_001377275.1(PER3):c.1278C>A (p.Ser426Arg)	PER3 (S107R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348130	NM_001377275.1(PER3):c.1318G>A (p.Ala440Thr)	PER3 (A440T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623993	NM_001377275.1(PER3):c.1358C>T (p.Thr453Met)	PER3 (T134M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398051	NM_001377275.1(PER3):c.1391A>G (p.Tyr464Cys)	PER3 (Y145C +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2245916	NM_001377275.1(PER3):c.1444A>G (p.Met482Val)	PER3 (M482V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204830	NM_001377275.1(PER3):c.1457C>T (p.Ser486Leu)	PER3 (S486L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607641	NM_001377275.1(PER3):c.1463A>C (p.Lys488Thr)	PER3 (K169T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342338	NM_001377275.1(PER3):c.1481G>A (p.Arg494His)	PER3 (R493H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482013	NM_001377275.1(PER3):c.1493A>G (p.Asn498Ser)	PER3 (N497S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318127	NM_001377275.1(PER3):c.1574T>C (p.Val525Ala)	PER3 (V525A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617019	NM_001377275.1(PER3):c.1594G>T (p.Asp532Tyr)	PER3 (D213Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359547	NM_001377275.1(PER3):c.1715A>C (p.Asn572Thr)	PER3 (N565T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607188	NM_001377275.1(PER3):c.1720A>G (p.Thr574Ala)	PER3 (T566A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211450	NM_001377275.1(PER3):c.2038G>A (p.Val680Met)	LOC126805604, PER3 (V673M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268712	NM_001377275.1(PER3):c.2123C>T (p.Ser708Leu)	LOC126805604, PER3 (S389L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411805	NM_001377275.1(PER3):c.2228G>A (p.Arg743Lys)	LOC126805604, PER3 (R424K +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2263245	NM_001377275.1(PER3):c.2234G>A (p.Gly745Glu)	LOC126805604, PER3 (G426E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272535	NM_001377275.1(PER3):c.2252A>G (p.Lys751Arg)	LOC126805604, PER3 (K744R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272536	NM_001377275.1(PER3):c.2278A>G (p.Ser760Gly)	LOC126805604, PER3 (S760G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613168	NM_001377275.1(PER3):c.2291G>T (p.Gly764Val)	LOC126805604, PER3 (G445V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474817	NM_001377275.1(PER3):c.2312C>T (p.Ala771Val)	LOC126805604, PER3 (A763V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244472	NM_001377275.1(PER3):c.2315A>G (p.His772Arg)	LOC126805604, PER3 (H453R +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2271434	NM_001377275.1(PER3):c.2366C>T (p.Ser789Leu)	LOC126805604, PER3 (S470L +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3211451	NM_001377275.1(PER3):c.2411C>T (p.Pro804Leu)	PER3, LOC126805604 (P804L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326027	NM_001377275.1(PER3):c.2432C>T (p.Pro811Leu)	LOC126805604, PER3 (P492L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223512	NM_001377275.1(PER3):c.2455G>A (p.Gly819Arg)	LOC126805604, PER3 (G819R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211452	NM_001377275.1(PER3):c.2501G>A (p.Gly834Glu)	LOC126805604, PER3 (G827E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638144	NM_001377275.1(PER3):c.2527C>T (p.Pro843Ser)	PER3, LOC126805604 (P524S +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2471873	NM_001377275.1(PER3):c.2534C>T (p.Pro845Leu)	LOC126805604, PER3 (P845L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312776	NM_001377275.1(PER3):c.2549C>A (p.Pro850His)	LOC126805604, PER3 (P842H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398582	NM_001377275.1(PER3):c.2584G>C (p.Asp862His)	LOC126805604, PER3 (D543H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315983	NM_001377275.1(PER3):c.2644A>G (p.Thr882Ala)	LOC126805604, PER3 (T874A +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2599576	NM_001377275.1(PER3):c.2657C>T (p.Ala886Val)	LOC126805604, PER3 (A878V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515213	NM_001377275.1(PER3):c.2680G>C (p.Ala894Pro)	LOC126805604, PER3 (A575P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216397	NM_001377275.1(PER3):c.2688T>G (p.Ser896Arg)	LOC126805604, PER3 (S889R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410012	NM_001377275.1(PER3):c.2696T>C (p.Leu899Pro)	LOC126805604, PER3 (L580P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211453	NM_001377275.1(PER3):c.2767C>A (p.Pro923Thr)	LOC126805604, PER3 (P923T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390087	NM_001377275.1(PER3):c.2849A>T (p.Asp950Val)	PER3 (D942V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267527	NM_001377275.1(PER3):c.2851C>A (p.Gln951Lys)	PER3 (Q943K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460685	NM_001377275.1(PER3):c.2908G>A (p.Gly970Ser)	PER3 (G970S +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2221497	NM_001377275.1(PER3):c.3116T>C (p.Leu1039Ser)	PER3 (L719S +5 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2598197	NM_001377275.1(PER3):c.3128G>A (p.Arg1043Lys)	PER3 (R1024K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 782902	NM_001377275.1(PER3):c.3146C>T (p.Thr1049Ile)	PER3 (T1023I +5 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2204574	NM_001377275.1(PER3):c.3149C>T (p.Ala1050Val)	PER3 (A1031V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568932	NM_001377275.1(PER3):c.3172C>T (p.Pro1058Ser)	PER3 (P1039S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3049280	NM_001377275.1(PER3):c.3181G>A (p.Glu1061Lys)	PER3 (E1035K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463860	NM_001377275.1(PER3):c.3197C>A (p.Thr1066Asn)	PER3 (T1058N +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292896	NM_001377275.1(PER3):c.3234A>G (p.Ile1078Met)	PER3 (I1052M +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511367	NM_001377275.1(PER3):c.3325G>A (p.Ala1109Thr)	PER3 (A1090T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211454	NM_001377275.1(PER3):c.3352C>T (p.Arg1118Trp)	PER3 (R1099W +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305809	NM_001377275.1(PER3):c.3368G>A (p.Arg1123His)	PER3 (R1097H +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305812	NM_001377275.1(PER3):c.3373C>T (p.Leu1125Phe)	PER3 (L1117F +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305816	NM_001377275.1(PER3):c.3380C>T (p.Thr1127Ile)	PER3 (T1101I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305814	NM_001377275.1(PER3):c.3514C>A (p.Gln1172Lys)	PER3 (Q1153K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386560	NM_001377275.1(PER3):c.3538A>G (p.Ile1180Val)	PER3 (I1154V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211455	NM_001377275.1(PER3):c.3556G>T (p.Val1186Phe)	PER3 (V1167F +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401724	NM_001377275.1(PER3):c.3559A>G (p.Thr1187Ala)	PER3 (T1178A +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404347	NM_001377275.1(PER3):c.3607C>A (p.Gln1203Lys)	PER3 (Q1177K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 87