PER2[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2255668	NM_022817.3(PER2):c.3616G>C (p.Ala1206Pro)	PER2 (A1206P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3257274	NM_022817.3(PER2):c.3534G>A (p.Arg1178=)	PER2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2380741	NM_022817.3(PER2):c.3449C>T (p.Thr1150Met)	PER2 (T1150M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211444	NM_022817.3(PER2):c.3420G>T (p.Met1140Ile)	PER2 (M1140I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2434649	NM_022817.3(PER2):c.3376C>T (p.His1126Tyr)	PER2 (H1126Y)	Single nucleotide variant (missense variant)	Advanced sleep phase syndrome 1	GUncertain significance
Select item 2212180	NM_022817.3(PER2):c.3374A>G (p.Glu1125Gly)	PER2 (E1125G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519125	NM_022817.3(PER2):c.3363G>A (p.Met1121Ile)	PER2 (M1121I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2631308	NM_022817.3(PER2):c.3275-1G>A	PER2	Single nucleotide variant (splice acceptor variant)	PER2-related disorder	GUncertain significance
Select item 376949	NM_022817.3(PER2):c.3250T>C (p.Cys1084Arg)	PER2 (C1084R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3305794	NM_022817.3(PER2):c.3061G>A (p.Asp1021Asn)	PER2 (D1021N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3049516	NM_022817.3(PER2):c.3012T>C (p.Thr1004=)	PER2	Single nucleotide variant (synonymous variant)	PER2-related disorder	GLikely benign
Select item 3211443	NM_022817.3(PER2):c.3002A>G (p.Glu1001Gly)	PER2 (E1001G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211442	NM_022817.3(PER2):c.2996C>T (p.Ala999Val)	PER2 (A999V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 634824	NM_022817.3(PER2):c.2963C>T (p.Pro988Leu)	PER2 (P988L)	Single nucleotide variant (missense variant)	Advanced sleep phase syndrome 1	GUncertain significance
Select item 3305798	NM_022817.3(PER2):c.2950C>A (p.Arg984Ser)	PER2 (R984S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3055231	NM_022817.3(PER2):c.2910_2936del (p.Ser971_Pro979del)	PER2	Deletion	PER2-related disorder	GLikely benign
Select item 2537925	NM_022817.3(PER2):c.2920G>A (p.Gly974Ser)	PER2 (G974S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255715	NM_022817.3(PER2):c.2888C>T (p.Pro963Leu)	PER2 (P963L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621951	NM_022817.3(PER2):c.2884T>C (p.Cys962Arg)	PER2 (C962R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544919	NM_022817.3(PER2):c.2861C>T (p.Ser954Leu)	PER2 (S954L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 735943	NM_022817.3(PER2):c.2859C>T (p.Thr953=)	PER2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3305801	NM_022817.3(PER2):c.2848C>T (p.Pro950Ser)	PER2 (P950S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3038758	NM_022817.3(PER2):c.2846T>A (p.Phe949Tyr)	PER2 (F949Y)	Single nucleotide variant (missense variant)	PER2-related disorder	GLikely benign
Select item 3211441	NM_022817.3(PER2):c.2845T>C (p.Phe949Leu)	PER2 (F949L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456220	NM_022817.3(PER2):c.2823G>A (p.Met941Ile)	PER2 (M941I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220065	NM_022817.3(PER2):c.2818G>A (p.Glu940Lys)	PER2 (E940K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275486	NM_022817.3(PER2):c.2804C>T (p.Pro935Leu)	PER2 (P935L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211440	NM_022817.3(PER2):c.2771T>C (p.Phe924Ser)	PER2 (F924S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211439	NM_022817.3(PER2):c.2770T>G (p.Phe924Val)	PER2 (F924V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318350	NM_022817.3(PER2):c.2721G>A (p.Met907Ile)	PER2 (M907I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211438	NM_022817.3(PER2):c.2683C>T (p.Pro895Ser)	PER2 (P895S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305793	NM_022817.3(PER2):c.2602C>T (p.Pro868Ser)	PER2 (P868S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354134	NM_022817.3(PER2):c.2593G>A (p.Val865Met)	PER2 (V865M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769600	NM_022817.3(PER2):c.2582C>T (p.Ala861Val)	PER2 (A861V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2434647	NM_022817.3(PER2):c.2542G>A (p.Ala848Thr)	PER2 (A848T)	Single nucleotide variant (missense variant)	Advanced sleep phase syndrome 1	GUncertain significance
Select item 3045417	NM_022817.3(PER2):c.2530G>T (p.Val844Leu)	PER2 (V844L)	Single nucleotide variant (missense variant)	PER2-related disorder	GLikely benign
Select item 787008	NM_022817.3(PER2):c.2466G>A (p.Pro822=)	PER2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3257675	NM_022817.3(PER2):c.2460G>A (p.Arg820=)	PER2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3048495	NM_022817.3(PER2):c.2448C>T (p.Pro816=)	PER2	Single nucleotide variant (synonymous variant)	PER2-related disorder	GLikely benign
Select item 3305795	NM_022817.3(PER2):c.2408A>G (p.Lys803Arg)	PER2 (K803R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2430006	NM_022817.3(PER2):c.2399A>G (p.Lys800Arg)	PER2 (K800R)	Single nucleotide variant (missense variant)	Autism spectrum disorder	GLikely benign
Select item 3211437	NM_022817.3(PER2):c.2323G>A (p.Ala775Thr)	PER2 (A775T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2652063	NM_022817.3(PER2):c.2318G>A (p.Arg773Gln)	PER2 (R773Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 746631	NM_022817.3(PER2):c.2304G>C (p.Gly768=)	PER2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2363280	NM_022817.3(PER2):c.2248A>C (p.Lys750Gln)	PER2 (K750Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305806	NM_022817.3(PER2):c.2234T>C (p.Phe745Ser)	PER2 (F745S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 770136	NM_022817.3(PER2):c.2185G>A (p.Val729Ile)	PER2 (V729I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3305802	NM_022817.3(PER2):c.2117G>T (p.Gly706Val)	PER2 (G706V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1050009	NM_022817.3(PER2):c.2114C>T (p.Ala705Val)	PER2 (A705V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3052018	NM_022817.3(PER2):c.2085G>A (p.Ala695=)	PER2	Single nucleotide variant (synonymous variant)	PER2-related disorder	GLikely benign
Select item 2474816	NM_022817.3(PER2):c.2084C>T (p.Ala695Val)	PER2 (A695V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3211435	NM_022817.3(PER2):c.2068A>G (p.Met690Val)	PER2 (M690V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464325	NM_022817.3(PER2):c.2048A>G (p.Lys683Arg)	PER2 (K683R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1278506	NM_022817.3(PER2):c.1995G>A (p.Ser665=)	PER2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3211434	NM_022817.3(PER2):c.1993T>C (p.Ser665Pro)	PER2 (S665P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3055371	NM_022817.3(PER2):c.1992G>A (p.Ala664=)	PER2	Single nucleotide variant (synonymous variant)	PER2-related disorder	GBenign
Select item 3043837	NM_022817.3(PER2):c.1991C>T (p.Ala664Val)	PER2 (A664V)	Single nucleotide variant (missense variant)	PER2-related disorder	GBenign
Select item 6345	NM_022817.3(PER2):c.1984A>G (p.Ser662Gly)	PER2 (S662G)	Single nucleotide variant (missense variant)	Advanced sleep phase syndrome 1	GPathogenic
Select item 3036487	NM_022817.3(PER2):c.1974C>T (p.Gly658=)	PER2	Single nucleotide variant (synonymous variant)	PER2-related disorder	GLikely benign
Select item 2623884	NM_022817.3(PER2):c.1972G>A (p.Gly658Ser)	PER2 (G658S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1246724	NM_022817.3(PER2):c.1965A>G (p.Ala655=)	PER2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3211433	NM_022817.3(PER2):c.1911G>A (p.Pro637=)	PER2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3211432	NM_022817.3(PER2):c.1894G>A (p.Ala632Thr)	PER2 (A632T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515084	NM_022817.3(PER2):c.1865G>A (p.Arg622Gln)	PER2 (R622Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3305796	NM_022817.3(PER2):c.1847T>C (p.Leu616Pro)	PER2 (L616P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 746968	NM_022817.3(PER2):c.1809G>A (p.Leu603=)	PER2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 977454	NM_022817.3(PER2):c.1793A>G (p.Asn598Ser)	PER2 (N598S)	Single nucleotide variant (missense variant)	Sleep abnormality	GUncertain significance
Select item 3035744	NM_022817.3(PER2):c.1775+4T>C	PER2	Single nucleotide variant (intron variant)	PER2-related disorder	GLikely benign
Select item 3305805	NM_022817.3(PER2):c.1768G>C (p.Val590Leu)	PER2 (V590L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266400	NM_022817.3(PER2):c.1656G>T (p.Lys552Asn)	PER2 (K552N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3058040	NM_022817.3(PER2):c.1635A>G (p.Gln545=)	PER2	Single nucleotide variant (synonymous variant)	PER2-related disorder	GLikely benign
Select item 3049581	NM_022817.3(PER2):c.1617A>G (p.Lys539=)	PER2	Single nucleotide variant (synonymous variant)	PER2-related disorder	GLikely benign
Select item 2551130	NM_022817.3(PER2):c.1592A>G (p.His531Arg)	PER2 (H531R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3046085	NM_022817.3(PER2):c.1542+4C>T	PER2	Single nucleotide variant (intron variant)	PER2-related disorder	GLikely benign
Select item 2257005	NM_022817.3(PER2):c.1528C>T (p.Arg510Cys)	PER2 (R510C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513052	NM_022817.3(PER2):c.1466G>A (p.Gly489Glu)	PER2 (G489E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401391	NM_022817.3(PER2):c.1463A>G (p.Asn488Ser)	PER2 (N488S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3050322	NM_022817.3(PER2):c.1446C>T (p.Tyr482=)	PER2	Single nucleotide variant (synonymous variant)	PER2-related disorder	GLikely benign
Select item 718810	NM_022817.3(PER2):c.1426C>A (p.His476Asn)	PER2 (H476N)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2264935	NM_022817.3(PER2):c.1418C>A (p.Pro473His)	PER2 (P473H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239854	NM_022817.3(PER2):c.1207C>T (p.Arg403Trp)	PER2 (R403W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2434646	NM_022817.3(PER2):c.1202G>A (p.Arg401His)	PER2 (R401H)	Single nucleotide variant (missense variant)	Advanced sleep phase syndrome 1	GUncertain significance
Select item 767874	NM_022817.3(PER2):c.1201C>T (p.Arg401Cys)	PER2 (R401C)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 714473	NM_022817.3(PER2):c.1179C>T (p.Phe393=)	PER2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2547963	NM_022817.3(PER2):c.1177T>C (p.Phe393Leu)	PER2 (F393L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3033141	NM_022817.3(PER2):c.1153+10C>G	PER2	Single nucleotide variant (intron variant)	PER2-related disorder	GLikely benign
Select item 731211	NM_022817.3(PER2):c.1095A>G (p.Pro365=)	PER2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2609029	NM_022817.3(PER2):c.1091C>T (p.Thr364Ile)	PER2 (T364I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2430007	NM_022817.3(PER2):c.958G>C (p.Gly320Arg)	PER2 (G320R)	Single nucleotide variant (missense variant)	Autism spectrum disorder	GLikely benign
Select item 3053684	NM_022817.3(PER2):c.945G>A (p.Glu315=)	PER2	Single nucleotide variant (synonymous variant)	PER2-related disorder	GLikely benign
Select item 2469585	NM_022817.3(PER2):c.896G>A (p.Arg299Gln)	PER2 (R299Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2278623	NM_022817.3(PER2):c.895C>T (p.Arg299Trp)	PER2 (R299W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296904	NM_022817.3(PER2):c.883C>G (p.Leu295Val)	PER2 (L295V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334062	NM_022817.3(PER2):c.871A>G (p.Met291Val)	PER2 (M291V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1335451	NM_022817.3(PER2):c.869G>A (p.Arg290His)	PER2 (R290H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2534132	NM_022817.3(PER2):c.868C>T (p.Arg290Cys)	PER2 (R290C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224424	NM_022817.3(PER2):c.844A>T (p.Asn282Tyr)	PER2 (N282Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 718246	NM_022817.3(PER2):c.825-5C>T	PER2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2516818	NM_022817.3(PER2):c.785A>C (p.Gln262Pro)	PER2 (Q262P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3211448	NM_022817.3(PER2):c.710G>A (p.Gly237Asp)	PER2 (G237D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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