ClinVar Miner

List of variants in gene ATR reported as likely benign for not specified

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Gene type:
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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_001184.4(ATR):c.7875G>A (p.Gln2625=) rs1802904 0.88595
NM_001184.4(ATR):c.5898+25T>G rs7620648 0.66679
NM_001184.4(ATR):c.1776T>A (p.Gly592=) rs2227930 0.63717
NM_001184.4(ATR):c.632T>C (p.Met211Thr) rs2227928 0.63625
NM_001184.4(ATR):c.5208T>C (p.Tyr1736=) rs2227931 0.34166
NM_001184.4(ATR):c.3726-47A>G rs73240314 0.13934
NM_001184.4(ATR):c.1885+39T>C rs73240318 0.10546
NM_001184.4(ATR):c.5460T>C (p.Tyr1820=) rs2227932 0.07623
NM_001184.4(ATR):c.3172-26T>A rs76852171 0.05061
NM_001184.4(ATR):c.4383-47A>G rs58348002 0.04498
NM_001184.4(ATR):c.5381-41C>T rs34502778 0.04288
NM_001184.4(ATR):c.3725+18A>G rs73864554 0.03416
NM_001184.4(ATR):c.5898+32A>G rs11719960 0.02829
NM_001184.4(ATR):c.4835A>G (p.Asn1612Ser) rs55894265 0.01275
NM_001184.4(ATR):c.891G>C (p.Lys297Asn) rs2229033 0.01036
NM_001184.4(ATR):c.6339A>G (p.Val2113=) rs7635479 0.00964
NM_001184.4(ATR):c.4820G>A (p.Ser1607Asn) rs55724025 0.00414
NM_001184.4(ATR):c.6394T>G (p.Tyr2132Asp) rs28910273 0.00349
NM_001184.4(ATR):c.2844A>C (p.Ala948=) rs147286949 0.00177
NM_001184.4(ATR):c.992A>G (p.Asp331Gly) rs150008448 0.00120
NM_001184.4(ATR):c.2776T>C (p.Phe926Leu) rs141783863 0.00119
NM_001184.4(ATR):c.2637C>T (p.Ala879=) rs150512706 0.00105
NM_001184.4(ATR):c.4200A>T (p.Leu1400=) rs150562945 0.00101
NM_001184.4(ATR):c.195C>T (p.Ser65=) rs139304565 0.00082
NM_001184.4(ATR):c.5931A>G (p.Gln1977=) rs150964938 0.00069
NM_001184.4(ATR):c.5601T>C (p.Leu1867=) rs138891875 0.00062
NM_001184.4(ATR):c.4677C>T (p.Asp1559=) rs112726878 0.00056
NM_001184.4(ATR):c.2946C>T (p.Phe982=) rs138061993 0.00037
NM_001184.4(ATR):c.2704T>C (p.Ser902Pro) rs146202702 0.00036
NM_001184.4(ATR):c.3241C>T (p.Leu1081=) rs139173669 0.00032
NM_001184.4(ATR):c.2205C>T (p.His735=) rs148955716 0.00029
NM_001184.4(ATR):c.117A>G (p.Gln39=) rs56297030 0.00023
NM_001184.4(ATR):c.483A>G (p.Arg161=) rs182268224 0.00021
NM_001184.4(ATR):c.4641+9A>G rs369284360 0.00015
NM_001184.4(ATR):c.3642T>C (p.His1214=) rs139078985 0.00011
NM_001184.4(ATR):c.2503T>C (p.Leu835=) rs377134163 0.00003
NM_001184.4(ATR):c.60-20G>T rs1285913916 0.00002
NM_001184.4(ATR):c.2157C>T (p.His719=) rs150161871 0.00001
NM_001184.4(ATR):c.2958T>C (p.Asp986=) rs143919996 0.00001
NM_001184.4(ATR):c.2979G>A (p.Arg993=) rs376960547 0.00001
NM_001184.4(ATR):c.4356A>G (p.Glu1452=) rs376297401 0.00001
NM_001184.4(ATR):c.5133C>T (p.Ser1711=) rs368178207 0.00001
NM_001184.4(ATR):c.624T>A (p.Thr208=) rs866939836 0.00001
NM_001184.4(ATR):c.7192+18T>C rs1349447137 0.00001
NM_001184.4(ATR):c.738C>T (p.Ser246=) rs755761580 0.00001
NM_001184.4(ATR):c.744A>C (p.Ala248=) rs368117837 0.00001
NM_001184.4(ATR):c.7899A>G (p.Leu2633=) rs147649584 0.00001
NM_001184.4(ATR):c.-29_-9delinsT rs1577732214
NM_001184.4(ATR):c.-6C>T rs769841006
NM_001184.4(ATR):c.2342-20T>C rs983859004
NM_001184.4(ATR):c.2805+12C>G rs778188323
NM_001184.4(ATR):c.3171+19A>G rs575077685
NM_001184.4(ATR):c.4383-19_4383-16del rs768981812
NM_001184.4(ATR):c.4852+21C>T rs587783332
NM_001184.4(ATR):c.5288+13A>C rs1553760235
NM_001184.4(ATR):c.6813A>G (p.Pro2271=) rs774286189
NM_001184.4(ATR):c.6898-15C>T rs1057524789
NM_001184.4(ATR):c.7185A>G (p.Lys2395=) rs749700431

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