ClinVar for MedGen (Select 12147) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065441	NM_000553.6(WRN):c.1720+1G>C	WRN	Single nucleotide variant (splice donor variant)	Werner syndrome	GLikely pathogenic
Select item 3024018	NM_000553.6(WRN):c.3692A>G (p.Asp1231Gly)	WRN (D1231G)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3022980	NM_000553.6(WRN):c.4113_4114dup (p.Arg1372fs)	WRN (R1372fs)	Duplication (frameshift variant)	Werner syndrome	GUncertain significance
Select item 3021958	NM_000553.6(WRN):c.3857C>A (p.Thr1286Lys)	WRN (T1286K)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3021114	NM_000553.6(WRN):c.2667A>G (p.Arg889=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 3019798	NM_000553.6(WRN):c.205A>G (p.Ile69Val)	WRN (I69V)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3019263	NM_000553.6(WRN):c.3411T>A (p.Ala1137=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome +1 more	GLikely benign
Select item 3018507	NM_000553.6(WRN):c.3459+19G>A	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 3018401	NM_000553.6(WRN):c.4143C>G (p.Ile1381Met)	WRN (I1381M)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3017427	NM_000553.6(WRN):c.877T>C (p.Tyr293His)	WRN (Y293H)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3014582	NM_000553.6(WRN):c.802C>A (p.Leu268Ile)	WRN (L268I)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3013294	NM_000553.6(WRN):c.2449-9T>C	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GUncertain significance
Select item 3012245	NM_000553.6(WRN):c.1146del (p.Lys382fs)	WRN (K382fs)	Deletion (frameshift variant)	Werner syndrome	GPathogenic
Select item 3011881	NM_000553.6(WRN):c.2313T>G (p.Cys771Trp)	WRN (C771W)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3011097	NM_000553.6(WRN):c.2967+7A>G	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 3010831	NM_000553.6(WRN):c.564G>A (p.Gln188=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 3009923	NM_000553.6(WRN):c.2314C>T (p.Pro772Ser)	WRN (P772S)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3008647	NM_000553.6(WRN):c.2031G>C (p.Gly677=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome +1 more	GLikely benign
Select item 3008320	NM_000553.6(WRN):c.3968C>G (p.Pro1323Arg)	WRN (P1323R)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3008115	NM_000553.6(WRN):c.3384-17T>G	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 3007987	NM_000553.6(WRN):c.3178A>G (p.Ser1060Gly)	WRN (S1060G)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3005890	NM_000553.6(WRN):c.2019T>C (p.Ile673=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome +1 more	GLikely benign
Select item 3004969	NM_000553.6(WRN):c.654+14G>A	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 3002790	NM_000553.6(WRN):c.1074T>C (p.Asp358=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 3002539	NM_000553.6(WRN):c.645T>A (p.Thr215=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 3002325	NM_000553.6(WRN):c.3163A>C (p.Asn1055His)	WRN (N1055H)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3002111	NM_000553.6(WRN):c.3598A>T (p.Arg1200Trp)	WRN (R1200W)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 3001883	NM_000553.6(WRN):c.2736C>T (p.Ile912=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GUncertain significance
Select item 3000362	NM_000553.6(WRN):c.3983-6T>G	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GUncertain significance
Select item 2998920	NM_000553.6(WRN):c.1033G>A (p.Glu345Lys)	WRN (E345K)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2998318	NM_000553.6(WRN):c.2273+19A>T	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2996963	NM_000553.6(WRN):c.3108A>G (p.Lys1036=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2996519	NM_000553.6(WRN):c.585C>T (p.Ile195=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2996216	NM_000553.6(WRN):c.2261T>C (p.Leu754Pro)	WRN (L754P)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2995934	NM_000553.6(WRN):c.1338G>A (p.Met446Ile)	WRN (M446I)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2995532	NM_000553.6(WRN):c.3101A>G (p.Tyr1034Cys)	WRN (Y1034C)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2994669	NM_000553.6(WRN):c.3139-4A>G	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GUncertain significance
Select item 2994196	NM_000553.6(WRN):c.505-20T>G	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2993000	NM_000553.6(WRN):c.2825+15T>C	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2992178	NM_000553.6(WRN):c.2732+11T>C	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2992110	NM_000553.6(WRN):c.249G>A (p.Met83Ile)	WRN (M83I)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2988817	NM_000553.6(WRN):c.1022A>G (p.His341Arg)	WRN (H341R)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2988566	NM_000553.6(WRN):c.3820-11T>C	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2987418	NM_000553.6(WRN):c.2066C>T (p.Ser689Phe)	WRN (S689F)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2985864	NM_000553.6(WRN):c.3766T>C (p.Ser1256Pro)	WRN (S1256P)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2985720	NM_000553.6(WRN):c.2526T>A (p.Pro842=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2984496	NM_000553.6(WRN):c.3459+20G>C	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2984206	NM_000553.6(WRN):c.1131A>G (p.Gly377=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2981451	NM_000553.6(WRN):c.2548C>G (p.Gln850Glu)	WRN (Q850E)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2979966	NM_000553.6(WRN):c.764C>G (p.Thr255Ser)	WRN (T255S)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2978763	NM_000553.6(WRN):c.4196C>T (p.Ser1399Leu)	LOC126860342, WRN (S1399L)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2978732	NM_000553.6(WRN):c.1981+20C>A	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2975562	NM_000553.6(WRN):c.1897T>C (p.Leu633=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GUncertain significance
Select item 2975045	NM_000553.6(WRN):c.707G>C (p.Arg236Thr)	WRN (R236T)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2975029	NM_000553.6(WRN):c.2521G>C (p.Ala841Pro)	WRN (A841P)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2974881	NM_000553.6(WRN):c.1867_1868del (p.Gln623fs)	WRN (Q623fs)	Microsatellite (frameshift variant)	Werner syndrome	GPathogenic
Select item 2974334	NM_000553.6(WRN):c.3466T>C (p.Leu1156=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2972679	NM_000553.6(WRN):c.1652+9_1652+11del	WRN	Deletion (intron variant)	Werner syndrome	GLikely benign
Select item 2972551	NM_000553.6(WRN):c.3460-17_3460-14del	WRN	Deletion (intron variant)	Werner syndrome	GLikely benign
Select item 2972192	NM_000553.6(WRN):c.3707C>T (p.Thr1236Ile)	WRN (T1236I)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2971073	NM_000553.6(WRN):c.823T>C (p.Leu275=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2968436	NM_000553.6(WRN):c.2613dup (p.Asp872fs)	WRN (D872fs)	Duplication (frameshift variant)	Werner syndrome	GPathogenic
Select item 2968434	NM_000553.6(WRN):c.2610T>A (p.Pro870=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2964132	NM_000553.6(WRN):c.1830-7C>G	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2960209	NM_000553.6(WRN):c.1981+13G>T	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2959463	NM_000553.6(WRN):c.3199G>A (p.Glu1067Lys)	WRN (E1067K)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2959322	NM_000553.6(WRN):c.2701A>G (p.Lys901Glu)	WRN (K901E)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2958914	NM_000553.6(WRN):c.1720+16G>A	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2956144	NM_000553.6(WRN):c.2234A>G (p.Asn745Ser)	WRN (N745S)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2955488	NM_000553.6(WRN):c.3008del (p.Leu1003fs)	WRN (L1003fs)	Deletion (frameshift variant)	Werner syndrome	GPathogenic
Select item 2920569	NM_000553.6(WRN):c.2967+17G>A	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2919946	NM_000553.6(WRN):c.1666G>A (p.Val556Met)	WRN (V556M)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2919741	NM_000553.6(WRN):c.2280C>T (p.His760=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2919205	NM_000553.6(WRN):c.2116G>T (p.Ala706Ser)	WRN (A706S)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2919014	NM_000553.6(WRN):c.2530G>T (p.Asp844Tyr)	WRN (D844Y)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2918586	NM_000553.6(WRN):c.2025G>T (p.Glu675Asp)	WRN (E675D)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2917941	NM_000553.6(WRN):c.3792T>C (p.Ser1264=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2917826	NM_000553.6(WRN):c.1346T>C (p.Leu449Pro)	WRN (L449P)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2917367	NM_000553.6(WRN):c.3459+20G>T	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2916951	NM_000553.6(WRN):c.2230G>A (p.Gly744Arg)	WRN (G744R)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2916586	NM_000553.6(WRN):c.3076G>A (p.Gly1026Arg)	WRN (G1026R)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2916049	NM_000553.6(WRN):c.3867G>T (p.Met1289Ile)	WRN (M1289I)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2915711	NM_000553.6(WRN):c.96+16A>G	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2914703	NM_000553.6(WRN):c.3572+13T>C	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2913776	NM_000553.6(WRN):c.3233+13G>T	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2913579	NM_000553.6(WRN):c.789T>C (p.Asp263=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2913121	NM_000553.6(WRN):c.504+13T>A	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2911399	NM_000553.6(WRN):c.3573-13T>C	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2910912	NM_000553.6(WRN):c.1467A>T (p.Pro489=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2910788	NM_000553.6(WRN):c.99A>T (p.Ala33=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2910336	NM_000553.6(WRN):c.3233+11C>T	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GLikely benign
Select item 2909972	NM_000553.6(WRN):c.3310-15T>C	WRN	Single nucleotide variant (intron variant)	Werner syndrome	GUncertain significance
Select item 2909862	NM_000553.6(WRN):c.2372G>C (p.Cys791Ser)	WRN (C791S)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2909779	NM_000553.6(WRN):c.2790G>A (p.Met930Ile)	WRN (M930I)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2909555	NM_000553.6(WRN):c.30A>C (p.Ala10=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2907994	NM_000553.6(WRN):c.1253C>T (p.Ala418Val)	WRN (A418V)	Single nucleotide variant (missense variant)	Werner syndrome	GUncertain significance
Select item 2906662	NM_000553.6(WRN):c.2058G>A (p.Lys686=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2906585	NM_000553.6(WRN):c.1721-17del	WRN	Deletion (intron variant)	Werner syndrome	GLikely benign
Select item 2905920	NM_000553.6(WRN):c.2676A>G (p.Lys892=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign
Select item 2905660	NM_000553.6(WRN):c.4116G>A (p.Arg1372=)	WRN	Single nucleotide variant (synonymous variant)	Werner syndrome	GLikely benign

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