ClinVar Miner

List of variants in gene ATR

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Gene type:
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Total variants: 220
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HGVS dbSNP
NM_001184.3(ATR):c.-91C>G rs189343119
NM_001184.4(ATR):c.*72T>G rs750327573
NM_001184.4(ATR):c.-29_-9delinsT rs886058060
NM_001184.4(ATR):c.-6C>T rs769841006
NM_001184.4(ATR):c.1006C>T (p.Arg336Trp) rs886058056
NM_001184.4(ATR):c.1170+148_1170+149insA
NM_001184.4(ATR):c.1170+150_1170+151insA
NM_001184.4(ATR):c.1318C>T (p.Pro440Ser) rs535140939
NM_001184.4(ATR):c.1326A>G (p.Lys442=) rs28897765
NM_001184.4(ATR):c.1328G>C (p.Arg443Thr) rs28367453
NM_001184.4(ATR):c.1349+289A>G
NM_001184.4(ATR):c.1350-3T>C rs587783323
NM_001184.4(ATR):c.1358_1359del (p.His453fs) rs886044646
NM_001184.4(ATR):c.151+4A>G rs1481733213
NM_001184.4(ATR):c.151+72G>A
NM_001184.4(ATR):c.152-9T>C rs748613519
NM_001184.4(ATR):c.1626A>G (p.Lys542=) rs762125386
NM_001184.4(ATR):c.1776T>A (p.Gly592=) rs2227930
NM_001184.4(ATR):c.1784C>T (p.Ser595Leu) rs747451103
NM_001184.4(ATR):c.1815T>C (p.Asp605=) rs2227929
NM_001184.4(ATR):c.1885+39T>C rs73240318
NM_001184.4(ATR):c.1885+7G>A rs74282951
NM_001184.4(ATR):c.1903C>T (p.Arg635Ter) rs1378333855
NM_001184.4(ATR):c.190A>G (p.Thr64Ala) rs35306038
NM_001184.4(ATR):c.1950G>A (p.Glu650=) rs28910270
NM_001184.4(ATR):c.195C>T (p.Ser65=) rs139304565
NM_001184.4(ATR):c.196G>A (p.Val66Met) rs758564083
NM_001184.4(ATR):c.2022A>G (p.Gly674=) rs587776690
NM_001184.4(ATR):c.2079-28T>C rs767195127
NM_001184.4(ATR):c.2092G>A (p.Asp698Asn) rs1553770633
NM_001184.4(ATR):c.2157C>T (p.His719=) rs150161871
NM_001184.4(ATR):c.2205C>T (p.His735=) rs148955716
NM_001184.4(ATR):c.2226T>C (p.Cys742=) rs147895945
NM_001184.4(ATR):c.2242A>G (p.Thr748Ala) rs879255363
NM_001184.4(ATR):c.225C>T (p.Ile75=) rs886058059
NM_001184.4(ATR):c.2290A>G (p.Lys764Glu) rs77208665
NM_001184.4(ATR):c.2320del (p.Ile774fs) rs757500301
NM_001184.4(ATR):c.2341+185G>A
NM_001184.4(ATR):c.2342-175A>G
NM_001184.4(ATR):c.2342-20T>C rs983859004
NM_001184.4(ATR):c.2442A>G (p.Glu814=) rs55895932
NM_001184.4(ATR):c.2503T>C (p.Leu835=) rs377134163
NM_001184.4(ATR):c.2532+4G>A rs190596919
NM_001184.4(ATR):c.2533-17T>C rs869312489
NM_001184.4(ATR):c.260G>T (p.Ser87Ile) rs200407265
NM_001184.4(ATR):c.2634-1G>A rs372271245
NM_001184.4(ATR):c.2634-74C>T
NM_001184.4(ATR):c.2637C>T (p.Ala879=) rs150512706
NM_001184.4(ATR):c.2653G>A (p.Val885Ile) rs141606250
NM_001184.4(ATR):c.2688G>A (p.Leu896=) rs117926957
NM_001184.4(ATR):c.268C>T (p.His90Tyr) rs28897763
NM_001184.4(ATR):c.2704T>C (p.Ser902Pro) rs146202702
NM_001184.4(ATR):c.2776T>C (p.Phe926Leu) rs141783863
NM_001184.4(ATR):c.2805+12C>G rs778188323
NM_001184.4(ATR):c.2805+272T>G
NM_001184.4(ATR):c.2844A>C (p.Ala948=) rs147286949
NM_001184.4(ATR):c.2875G>A (p.Val959Met) rs28910271
NM_001184.4(ATR):c.289A>T (p.Ile97Phe) rs138473993
NM_001184.4(ATR):c.292+15T>G rs886058058
NM_001184.4(ATR):c.292+745A>C rs78050501
NM_001184.4(ATR):c.293-20C>T rs115097590
NM_001184.4(ATR):c.2958T>C (p.Asp986=) rs143919996
NM_001184.4(ATR):c.2979G>A (p.Arg993=) rs376960547
NM_001184.4(ATR):c.305G>T (p.Trp102Leu) rs794727632
NM_001184.4(ATR):c.3120G>A (p.Leu1040=) rs28910272
NM_001184.4(ATR):c.3152G>A (p.Arg1051His)
NM_001184.4(ATR):c.3171+132A>G
NM_001184.4(ATR):c.3171+19A>G rs575077685
NM_001184.4(ATR):c.3171+1G>A rs199731535
NM_001184.4(ATR):c.3172-266C>A rs143205618
NM_001184.4(ATR):c.3172-26T>A rs76852171
NM_001184.4(ATR):c.3241C>T (p.Leu1081=) rs139173669
NM_001184.4(ATR):c.325C>T (p.Arg109Trp) rs146405935
NM_001184.4(ATR):c.3358-1899T>G rs869312482
NM_001184.4(ATR):c.3424A>G (p.Ser1142Gly) rs149008479
NM_001184.4(ATR):c.3450+567A>G rs564240158
NM_001184.4(ATR):c.3451-641C>A rs373891058
NM_001184.4(ATR):c.3477G>T (p.Met1159Ile) rs587777851
NM_001184.4(ATR):c.3497A>C (p.His1166Pro) rs201438783
NM_001184.4(ATR):c.3581+486T>C rs72996190
NM_001184.4(ATR):c.3582-302T>C
NM_001184.4(ATR):c.3614A>G (p.His1205Arg) rs1553767201
NM_001184.4(ATR):c.3642T>C (p.His1214=) rs139078985
NM_001184.4(ATR):c.3725+18A>G rs73864554
NM_001184.4(ATR):c.3726-24C>A rs869312487
NM_001184.4(ATR):c.3726-47A>G rs73240314
NM_001184.4(ATR):c.3799G>A (p.Val1267Ile) rs377689383
NM_001184.4(ATR):c.3819+389T>C rs559805028
NM_001184.4(ATR):c.3945+2dup rs537031994
NM_001184.4(ATR):c.3945+483G>A rs149815404
NM_001184.4(ATR):c.3946-104A>G rs869312483
NM_001184.4(ATR):c.3952del (p.Lys1317_Leu1318insTer) rs869312789
NM_001184.4(ATR):c.4002G>A (p.Gln1334=) rs56026468
NM_001184.4(ATR):c.4153-10del rs112116713
NM_001184.4(ATR):c.4153-21dup rs112116713
NM_001184.4(ATR):c.4200A>T (p.Leu1400=) rs150562945
NM_001184.4(ATR):c.4218G>A (p.Ala1406=) rs770181975
NM_001184.4(ATR):c.423T>C (p.Ile141=) rs10935466
NM_001184.4(ATR):c.4266+120A>T
NM_001184.4(ATR):c.4306A>G (p.Asn1436Asp) rs587783328
NM_001184.4(ATR):c.431T>G (p.Val144Gly) rs749942139
NM_001184.4(ATR):c.4323A>G (p.Gln1441=) rs56100509
NM_001184.4(ATR):c.4351C>T (p.Arg1451Trp) rs148064542
NM_001184.4(ATR):c.4356A>G (p.Glu1452=) rs376297401
NM_001184.4(ATR):c.436A>G (p.Thr146Ala) rs765018743
NM_001184.4(ATR):c.4376A>G (p.Asn1459Ser) rs144591613
NM_001184.4(ATR):c.437C>A (p.Thr146Lys) rs368592452
NM_001184.4(ATR):c.4382+6T>C rs758074436
NM_001184.4(ATR):c.4383-177C>T
NM_001184.4(ATR):c.4383-19_4383-16del rs768981812
NM_001184.4(ATR):c.4383-232G>T
NM_001184.4(ATR):c.4383-47A>G rs58348002
NM_001184.4(ATR):c.4405A>G (p.Thr1469Ala) rs78895258
NM_001184.4(ATR):c.4407C>T (p.Thr1469=) rs201300027
NM_001184.4(ATR):c.4503+247A>G
NM_001184.4(ATR):c.4504-263T>A
NM_001184.4(ATR):c.4509A>T (p.Arg1503=) rs398123602
NM_001184.4(ATR):c.4576A>G (p.Ile1526Val) rs34124242
NM_001184.4(ATR):c.4641+15C>T rs200619976
NM_001184.4(ATR):c.4641+1G>T rs797045403
NM_001184.4(ATR):c.4641+9A>G rs369284360
NM_001184.4(ATR):c.4677C>T (p.Asp1559=) rs112726878
NM_001184.4(ATR):c.4764C>T (p.Leu1588=) rs142240637
NM_001184.4(ATR):c.4820G>A (p.Ser1607Asn) rs55724025
NM_001184.4(ATR):c.4835A>G (p.Asn1612Ser) rs55894265
NM_001184.4(ATR):c.483A>G (p.Arg161=) rs182268224
NM_001184.4(ATR):c.4846T>G (p.Ser1616Ala) rs201492267
NM_001184.4(ATR):c.4852+21C>T rs587783332
NM_001184.4(ATR):c.4852+256T>C
NM_001184.4(ATR):c.489T>C (p.Asn163=) rs886058057
NM_001184.4(ATR):c.4957C>T (p.Arg1653Ter) rs778813551
NM_001184.4(ATR):c.4995G>T (p.Lys1665Asn) rs1553761113
NM_001184.4(ATR):c.5052T>C (p.His1684=) rs150810277
NM_001184.4(ATR):c.5133C>T (p.Ser1711=) rs368178207
NM_001184.4(ATR):c.5196+109G>A
NM_001184.4(ATR):c.5196+1G>A rs1553760567
NM_001184.4(ATR):c.5197-289A>G
NM_001184.4(ATR):c.5208T>C (p.Tyr1736=) rs2227931
NM_001184.4(ATR):c.5257A>G (p.Ile1753Val) rs143806447
NM_001184.4(ATR):c.5288+130G>A
NM_001184.4(ATR):c.5288+13A>C rs1553760235
NM_001184.4(ATR):c.5288+248T>C
NM_001184.4(ATR):c.5305G>C (p.Glu1769Gln) rs376811787
NM_001184.4(ATR):c.5349G>T (p.Gln1783His) rs886058055
NM_001184.4(ATR):c.5380+121C>A
NM_001184.4(ATR):c.5380+341A>T rs869312490
NM_001184.4(ATR):c.5381-41C>T rs34502778
NM_001184.4(ATR):c.5460T>C (p.Tyr1820=) rs2227932
NM_001184.4(ATR):c.5572T>C (p.Cys1858Arg) rs367898142
NM_001184.4(ATR):c.5601T>C (p.Leu1867=) rs138891875
NM_001184.4(ATR):c.5635G>T (p.Asp1879Tyr) rs387907327
NM_001184.4(ATR):c.5732A>G (p.Asn1911Ser) rs587783334
NM_001184.4(ATR):c.5739-11_5739-4del rs797045404
NM_001184.4(ATR):c.5739-14G>T rs587783335
NM_001184.4(ATR):c.5739-14_5739-6delinsT rs886058054
NM_001184.4(ATR):c.5739-14_5739-7del rs878853001
NM_001184.4(ATR):c.5739-14_5739-9del rs72272981
NM_001184.4(ATR):c.5739-7_5739-6del rs72371423
NM_001184.4(ATR):c.5868C>T (p.Tyr1956=) rs112018640
NM_001184.4(ATR):c.5898+25T>G rs7620648
NM_001184.4(ATR):c.5898+32A>G rs11719960
NM_001184.4(ATR):c.5899-8del rs538488507
NM_001184.4(ATR):c.59+1024G>A rs6788362
NM_001184.4(ATR):c.59+3019A>C rs75518582
NM_001184.4(ATR):c.59+4G>A rs758046042
NM_001184.4(ATR):c.5900G>A (p.Gly1967Asp) rs751198306
NM_001184.4(ATR):c.5931A>G (p.Gln1977=) rs150964938
NM_001184.4(ATR):c.5987T>C (p.Met1996Thr) rs150339560
NM_001184.4(ATR):c.60-20G>T rs1285913916
NM_001184.4(ATR):c.60-51A>T
NM_001184.4(ATR):c.6078+10T>C rs762754313
NM_001184.4(ATR):c.6079-14G>A rs886058053
NM_001184.4(ATR):c.6090G>A (p.Ala2030=) rs201988169
NM_001184.4(ATR):c.6197G>A (p.Arg2066Gln) rs886058052
NM_001184.4(ATR):c.6221+2962T>C rs869312488
NM_001184.4(ATR):c.6221+3G>A rs200980335
NM_001184.4(ATR):c.6226C>G (p.Leu2076Val) rs372864251
NM_001184.4(ATR):c.624T>A (p.Thr208=) rs866939836
NM_001184.4(ATR):c.6259A>G (p.Met2087Val) rs757353909
NM_001184.4(ATR):c.632T>C (p.Met211Thr) rs2227928
NM_001184.4(ATR):c.6339A>G (p.Val2113=) rs7635479
NM_001184.4(ATR):c.6394T>G (p.Tyr2132Asp) rs28910273
NM_001184.4(ATR):c.6431A>G (p.Gln2144Arg) rs387906797
NM_001184.4(ATR):c.6553-490C>G rs749552840
NM_001184.4(ATR):c.6687+210T>G rs869312485
NM_001184.4(ATR):c.6687+262A>G
NM_001184.4(ATR):c.6813A>G (p.Pro2271=) rs774286189
NM_001184.4(ATR):c.6896T>C (p.Met2299Thr) rs145119827
NM_001184.4(ATR):c.6897+464C>G rs587777852
NM_001184.4(ATR):c.6898-15C>T rs1057524789
NM_001184.4(ATR):c.6898-69G>A rs115906468
NM_001184.4(ATR):c.6960G>A (p.Lys2320=) rs752654793
NM_001184.4(ATR):c.6961T>C (p.Phe2321Leu) rs587783338
NM_001184.4(ATR):c.7041+4G>C rs113544835
NM_001184.4(ATR):c.7041+8G>A rs201106004
NM_001184.4(ATR):c.7185A>G (p.Lys2395=) rs749700431
NM_001184.4(ATR):c.7192+18T>C rs1349447137
NM_001184.4(ATR):c.7192+98A>G rs78659656
NM_001184.4(ATR):c.7220G>A (p.Arg2407His) rs778835776
NM_001184.4(ATR):c.7274G>A (p.Arg2425Gln) rs2229032
NM_001184.4(ATR):c.7300C>G (p.Pro2434Ala) rs33972295
NM_001184.4(ATR):c.7356_7358TAG[3] (p.Ser2453dup) rs756975919
NM_001184.4(ATR):c.738C>T (p.Ser246=) rs755761580
NM_001184.4(ATR):c.744A>C (p.Ala248=) rs368117837
NM_001184.4(ATR):c.7471G>A (p.Val2491Ile) rs556313656
NM_001184.4(ATR):c.7655+169A>C
NM_001184.4(ATR):c.7667C>G (p.Thr2556Ser) rs200490116
NM_001184.4(ATR):c.7725G>A (p.Ala2575=) rs587783340
NM_001184.4(ATR):c.7761+375C>T rs11717703
NM_001184.4(ATR):c.7762-174A>G
NM_001184.4(ATR):c.7762-208T>C rs552872123
NM_001184.4(ATR):c.7762-209G>T rs577916091
NM_001184.4(ATR):c.7762-439T>C rs869312484
NM_001184.4(ATR):c.7762-724C>T rs869312486
NM_001184.4(ATR):c.7875G>A (p.Gln2625=) rs1802904
NM_001184.4(ATR):c.7902C>T (p.Cys2634=)
NM_001184.4(ATR):c.816A>G (p.Ser272=) rs34685245
NM_001184.4(ATR):c.891G>C (p.Lys297Asn) rs2229033
NM_001184.4(ATR):c.946G>A (p.Val316Ile) rs28897764
NM_001184.4(ATR):c.992A>G (p.Asp331Gly) rs150008448

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