ClinVar Miner

List of variants in gene ATR reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 95
Download table as spreadsheet
HGVS dbSNP
NM_001184.4(ATR):c.-29_-9delinsT rs886058060
NM_001184.4(ATR):c.-6C>T rs769841006
NM_001184.4(ATR):c.1326A>G (p.Lys442=) rs28897765
NM_001184.4(ATR):c.1776T>A (p.Gly592=) rs2227930
NM_001184.4(ATR):c.1885+39T>C rs73240318
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.2079-28T>C rs767195127
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.2290A>G (p.Lys764Glu) rs77208665
NM_001184.4(ATR):c.2342-20T>C rs983859004
NM_001184.4(ATR):c.2442A>G (p.Glu814=) rs55895932
NM_001184.4(ATR):c.2533-17T>C rs869312489
NM_001184.4(ATR):c.2637C>T (p.Ala879=) rs150512706
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.2844A>C (p.Ala948=) rs147286949
NM_001184.4(ATR):c.2875G>A (p.Val959Met) rs28910271
NM_001184.4(ATR):c.292+745A>C rs78050501
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.3120G>A (p.Leu1040=) rs28910272
NM_001184.4(ATR):c.3171+19A>G rs575077685
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.3358-1899T>G rs869312482
NM_001184.4(ATR):c.3450+567A>G rs564240158
NM_001184.4(ATR):c.3451-641C>A rs373891058
NM_001184.4(ATR):c.3581+486T>C rs72996190
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.3819+389T>C rs559805028
NM_001184.4(ATR):c.3945+483G>A rs149815404
NM_001184.4(ATR):c.3946-104A>G rs869312483
NM_001184.4(ATR):c.4002G>A (p.Gln1334=) rs56026468
NM_001184.4(ATR):c.4200A>T (p.Leu1400=) rs150562945
NM_001184.4(ATR):c.423T>C (p.Ile141=) rs10935466
NM_001184.4(ATR):c.4356A>G (p.Glu1452=) rs376297401
NM_001184.4(ATR):c.4383-19_4383-16del rs768981812
NM_001184.4(ATR):c.4383-47A>G rs58348002
NM_001184.4(ATR):c.4641+9A>G rs369284360
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.4852+21C>T rs587783332
NM_001184.4(ATR):c.5133C>T (p.Ser1711=) rs368178207
NM_001184.4(ATR):c.5208T>C (p.Tyr1736=) rs2227931
NM_001184.4(ATR):c.5288+13A>C rs1553760235
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.5601T>C (p.Leu1867=) rs138891875
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.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.5931A>G (p.Gln1977=) rs150964938
NM_001184.4(ATR):c.60-20G>T rs1285913916
NM_001184.4(ATR):c.6221+2962T>C rs869312488
NM_001184.4(ATR):c.624T>A (p.Thr208=) rs866939836
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.6553-490C>G rs749552840
NM_001184.4(ATR):c.6687+210T>G rs869312485
NM_001184.4(ATR):c.6813A>G (p.Pro2271=) rs774286189
NM_001184.4(ATR):c.6898-15C>T rs1057524789
NM_001184.4(ATR):c.6898-69G>A rs115906468
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.7274G>A (p.Arg2425Gln) rs2229032
NM_001184.4(ATR):c.7300C>G (p.Pro2434Ala) rs33972295
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.7761+375C>T rs11717703
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.