ClinVar Miner

List of variants in gene ATR reported as likely benign by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
Download table as spreadsheet
HGVS dbSNP
NM_001184.4(ATR):c.1776T>A (p.Gly592=) rs2227930
NM_001184.4(ATR):c.1885+39T>C rs73240318
NM_001184.4(ATR):c.195C>T (p.Ser65=) rs139304565
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.2637C>T (p.Ala879=) rs150512706
NM_001184.4(ATR):c.2844A>C (p.Ala948=) rs147286949
NM_001184.4(ATR):c.3172-26T>A rs76852171
NM_001184.4(ATR):c.3725+18A>G rs73864554
NM_001184.4(ATR):c.3726-47A>G rs73240314
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.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.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.5208T>C (p.Tyr1736=) rs2227931
NM_001184.4(ATR):c.5381-41C>T rs34502778
NM_001184.4(ATR):c.5460T>C (p.Tyr1820=) rs2227932
NM_001184.4(ATR):c.5898+25T>G rs7620648
NM_001184.4(ATR):c.5898+32A>G rs11719960
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.7875G>A (p.Gln2625=) rs1802904
NM_001184.4(ATR):c.891G>C (p.Lys297Asn) rs2229033

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.