ClinVar for Gene (Select 545) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3061440	NM_001184.4(ATR):c.4125A>G (p.Glu1375=)	ATR	Single nucleotide variant (synonymous variant)	ATR-related condition	GLikely benign
Select item 3054537	NM_001184.4(ATR):c.6897+458_6897+459insTAGT	ATR	Insertion (intron variant)	ATR-related condition	GLikely benign
Select item 3040863	NM_001184.4(ATR):c.7041+7A>G	ATR	Single nucleotide variant (intron variant)	ATR-related condition	GLikely benign
Select item 3036115	NM_001184.4(ATR):c.-10C>T	ATR	Single nucleotide variant (5 prime UTR variant)	ATR-related condition	GLikely benign
Select item 3026412	NM_001184.4(ATR):c.4672C>G (p.His1558Asp)	ATR (H1494D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3023268	NM_001184.4(ATR):c.224T>C (p.Ile75Thr)	ATR (I75T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3021819	NM_001184.4(ATR):c.932G>A (p.Arg311Lys)	ATR (R311K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3019901	NM_001184.4(ATR):c.3582-8T>G	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011635	NM_001184.4(ATR):c.138del (p.Asp47fs)	ATR (D47fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 3009826	NM_001184.4(ATR):c.2299C>A (p.Leu767Ile)	ATR (L767I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3009109	NM_001184.4(ATR):c.2532+8A>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3007382	NM_001184.4(ATR):c.2806-12T>A	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005278	NM_001184.4(ATR):c.6898-34_6898-20del	ATR	Deletion (intron variant)	not provided	GLikely benign
Select item 3003811	NM_001184.4(ATR):c.383G>T (p.Cys128Phe)	ATR (C128F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2999960	NM_001184.4(ATR):c.3306C>T (p.Ser1102=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2999218	NM_001184.4(ATR):c.151+11A>T	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2997541	NM_001184.4(ATR):c.3358-20T>G	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2996743	NM_001184.4(ATR):c.3581+17G>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2996630	NM_001184.4(ATR):c.4406C>T (p.Thr1469Ile)	ATR (T1405I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2996377	NM_001184.4(ATR):c.2634-16T>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2993569	NM_001184.4(ATR):c.7193-19A>G	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2992214	NM_001184.4(ATR):c.6199T>C (p.Tyr2067His)	ATR, LOC126806830 (Y2067H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2992182	NM_001184.4(ATR):c.1295G>A (p.Arg432His)	ATR (R432H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2986244	NM_001184.4(ATR):c.2342-6C>T	ATR	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2981928	NM_001184.4(ATR):c.33G>T (p.Met11Ile)	ATR, LOC129937703 (M11I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2980472	NM_001184.4(ATR):c.3726-8_3726-5del	ATR	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2980223	NM_001184.4(ATR):c.2994A>C (p.Leu998=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977805	NM_001184.4(ATR):c.6828C>T (p.Thr2276=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2972428	NM_001184.4(ATR):c.6525A>T (p.Ala2175=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2971069	NM_001184.4(ATR):c.2341+15C>G	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2968505	NM_001184.4(ATR):c.3565C>T (p.Pro1189Ser)	ATR (P1125S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2964764	NM_001184.4(ATR):c.7503+7G>A	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2963401	NM_001184.4(ATR):c.7784T>C (p.Ile2595Thr)	ATR (I2595T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2960208	NM_001184.4(ATR):c.6079-16A>G	ATR, LOC126806830	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2959323	NM_001184.4(ATR):c.6079-5dup	ATR, LOC126806830	Duplication (intron variant)	not provided	GBenign
Select item 2956241	NM_001184.4(ATR):c.2788A>G (p.Lys930Glu)	ATR (K866E +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2919109	NM_001184.4(ATR):c.7025A>G (p.Asn2342Ser)	ATR (N2278S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2918385	NM_001184.4(ATR):c.151+12A>G	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2917645	NM_001184.4(ATR):c.4152+19G>A	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2917601	NM_001184.4(ATR):c.1951T>G (p.Trp651Gly)	ATR (W587G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2916681	NM_001184.4(ATR):c.997G>A (p.Val333Met)	ATR (V333M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2916540	NM_001184.4(ATR):c.2028dup (p.Ile677fs)	ATR (I613fs +1 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 2916369	NM_001184.4(ATR):c.5381-16T>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2916019	NM_001184.4(ATR):c.6924A>G (p.Lys2308=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2914888	NM_001184.4(ATR):c.6138T>C (p.Tyr2046=)	ATR, LOC126806830	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2913925	NM_001184.4(ATR):c.2805+20T>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2913677	NM_001184.4(ATR):c.7459A>G (p.Thr2487Ala)	ATR (T2423A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2912041	NM_001184.4(ATR):c.1585T>C (p.Ser529Pro)	ATR (S529P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2911937	NM_001184.4(ATR):c.5204A>G (p.His1735Arg)	ATR (H1671R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2911847	NM_001184.4(ATR):c.6334C>T (p.Arg2112Cys)	ATR (R2048C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2911801	NM_001184.4(ATR):c.6078+13A>G	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2911506	NM_001184.4(ATR):c.1541+17G>A	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2911413	NM_001184.4(ATR):c.1171-20A>G	ATR	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2910060	NM_001184.4(ATR):c.5643A>G (p.Leu1881=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2910033	NM_001184.4(ATR):c.634G>C (p.Val212Leu)	ATR (V212L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2908622	NM_001184.4(ATR):c.5008C>G (p.Gln1670Glu)	ATR (Q1606E +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2905320	NM_001184.4(ATR):c.2638G>T (p.Ala880Ser)	ATR (A816S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2901082	NM_001184.4(ATR):c.3694G>T (p.Ala1232Ser)	ATR (A1168S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2899768	NM_001184.4(ATR):c.2165_2167del (p.Phe722del)	ATR (F722del +1 more)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2898974	NM_001184.4(ATR):c.361A>G (p.Lys121Glu)	ATR (K121E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2896712	NM_001184.4(ATR):c.6552+9G>T	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2895618	NM_001184.4(ATR):c.6898-11T>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2892365	NM_001184.4(ATR):c.6608A>G (p.His2203Arg)	ATR (H2203R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2891973	NM_001184.4(ATR):c.4266+7G>A	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2891774	NM_001184.4(ATR):c.7900T>G (p.Cys2634Gly)	ATR (C2570G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2890454	NM_001184.4(ATR):c.4503+19T>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2890225	NM_001184.4(ATR):c.6443G>A (p.Arg2148Gln)	ATR (R2148Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2888672	NM_001184.4(ATR):c.6080A>G (p.Asp2027Gly)	ATR, LOC126806830 (D2027G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2885684	NM_001184.4(ATR):c.2168A>G (p.Tyr723Cys)	ATR (Y659C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2884833	NM_001184.4(ATR):c.1885+9T>G	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2883531	NM_001184.4(ATR):c.6001C>T (p.Arg2001Ter)	ATR (R1937* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2883238	NM_001184.4(ATR):c.2633+13G>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2883233	NM_001184.4(ATR):c.4641+19C>T	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2883040	NM_001184.4(ATR):c.2633+13G>A	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2882425	NM_001184.4(ATR):c.83C>T (p.Thr28Ile)	ATR (T28I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2878662	NM_001184.4(ATR):c.963G>A (p.Leu321=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2871307	NM_001184.4(ATR):c.5380G>A (p.Asp1794Asn)	ATR (D1730N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2871024	NM_001184.4(ATR):c.3358-17_3358-16del	ATR	Deletion (intron variant)	not provided	GLikely benign
Select item 2870731	NM_001184.4(ATR):c.7504-18A>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869082	NM_001184.4(ATR):c.1541+7C>G	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2865269	NM_001184.4(ATR):c.7182T>C (p.Tyr2394=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2865062	NM_001184.4(ATR):c.3879A>G (p.Gln1293=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2864133	NM_001184.4(ATR):c.7087C>T (p.Arg2363Ter)	ATR (R2299* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2862189	NM_001184.4(ATR):c.7016T>A (p.Met2339Lys)	ATR (M2275K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2860511	NM_001184.4(ATR):c.5559-12A>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2860091	NM_001184.4(ATR):c.6685C>A (p.Pro2229Thr)	ATR (P2165T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2859189	NM_001184.4(ATR):c.4353G>A (p.Arg1451=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2855192	NM_001184.4(ATR):c.1304G>C (p.Ser435Thr)	ATR (S435T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2854941	NM_001184.4(ATR):c.284G>A (p.Ser95Asn)	ATR (S95N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2851856	NM_001184.4(ATR):c.2669T>G (p.Leu890Ter)	ATR (L826* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2851394	NM_001184.4(ATR):c.74A>C (p.Glu25Ala)	ATR (E25A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2851218	NM_001184.4(ATR):c.151+9C>G	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2850707	NM_001184.4(ATR):c.5197-13T>A	ATR	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2850353	NM_001184.4(ATR):c.4267-14A>C	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2849376	NM_001184.4(ATR):c.1732+8C>T	ATR	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2849290	NM_001184.4(ATR):c.1350-25CT[2]	ATR	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2846500	NM_001184.4(ATR):c.5836A>G (p.Asn1946Asp)	ATR (N1882D +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2846497	NM_001184.4(ATR):c.451del (p.Gln151fs)	ATR (Q151fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2845868	NM_001184.4(ATR):c.3688dup (p.Thr1230fs)	ATR (T1166fs +1 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 2842781	NM_001184.4(ATR):c.4259C>G (p.Ala1420Gly)	ATR (A1420G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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