ClinVar Miner

List of variants in gene ATR reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 94
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HGVS dbSNP gnomAD frequency
NM_001184.4(ATR):c.5288+248T>C rs9856772 0.91892
NM_001184.4(ATR):c.7875G>A (p.Gln2625=) rs1802904 0.88595
NM_001184.4(ATR):c.4852+256T>C rs9876254 0.67368
NM_001184.4(ATR):c.5898+25T>G rs7620648 0.66679
NM_001184.4(ATR):c.4503+247A>G rs6791816 0.64124
NM_001184.4(ATR):c.4383-232G>T rs9855919 0.64078
NM_001184.4(ATR):c.2805+272T>G rs10935465 0.64051
NM_001184.4(ATR):c.2634-74C>T rs9869842 0.63734
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.1349+289A>G rs6440089 0.63227
NM_001184.4(ATR):c.5898+82del rs377263877 0.58688
NM_001184.4(ATR):c.5898+81T>A rs201323437 0.56282
NM_001184.4(ATR):c.2341+185G>A rs7641914 0.41727
NM_001184.4(ATR):c.5208T>C (p.Tyr1736=) rs2227931 0.34166
NM_001184.4(ATR):c.5288+130G>A rs11916455 0.34154
NM_001184.4(ATR):c.4504-263T>A rs6440085 0.34112
NM_001184.4(ATR):c.1815T>C (p.Asp605=) rs2227929 0.33689
NM_001184.4(ATR):c.2342-175A>G rs13070239 0.33666
NC_000003.12:g.142449134A>G rs10935463 0.33436
NM_001184.4(ATR):c.5898+67_5898+79del rs201603669 0.28696
NM_001184.4(ATR):c.5898+70A>G rs13093790 0.26341
NM_001184.4(ATR):c.5898+54A>G rs74677466 0.19240
NM_001184.4(ATR):c.5898+68A>G rs192732571 0.19130
NM_001184.4(ATR):c.3357+128G>A rs13091637 0.16442
NM_001184.4(ATR):c.4383-177C>T rs10804682 0.14718
NM_001184.4(ATR):c.3726-47A>G rs73240314 0.13934
NM_001184.4(ATR):c.1170+148_1170+149insA rs201956927 0.13887
NM_001184.4(ATR):c.1170+150_1170+151insA rs200943610 0.13612
NM_001184.4(ATR):c.7274G>A (p.Arg2425Gln) rs2229032 0.12815
NM_001184.4(ATR):c.1885+39T>C rs73240318 0.10546
NM_001184.4(ATR):c.7762-174A>G rs7652760 0.09765
NM_001184.4(ATR):c.1885+67T>C rs9990092 0.09560
NM_001184.4(ATR):c.5898+69_5898+79del rs1559937368 0.08107
NM_001184.4(ATR):c.5898+51_5898+79del rs1559937374 0.07639
NM_001184.4(ATR):c.5460T>C (p.Tyr1820=) rs2227932 0.07623
NM_001184.4(ATR):c.5197-289A>G rs7618253 0.07373
NM_001184.4(ATR):c.60-51A>T rs62276447 0.07197
NM_001184.4(ATR):c.5380+121C>A rs11927681 0.07056
NM_001184.4(ATR):c.3450+168C>T rs11920625 0.06276
NM_001184.4(ATR):c.5898+71_5898+79del rs1559937364 0.05952
NM_001184.4(ATR):c.5898+56A>G rs868522344 0.05816
NM_001184.4(ATR):c.3172-26T>A rs76852171 0.05061
NM_001184.4(ATR):c.5898+58A>G rs71619398 0.04601
NM_001184.4(ATR):c.2442A>G (p.Glu814=) rs55895932 0.04528
NM_001184.4(ATR):c.5196+109G>A rs148397694 0.04526
NM_001184.4(ATR):c.4383-47A>G rs58348002 0.04498
NM_001184.4(ATR):c.1885+63C>T rs201864026 0.04373
NM_001184.4(ATR):c.151+72G>A rs79601680 0.04357
NM_001184.4(ATR):c.3171+132A>G rs75957718 0.04356
NM_001184.4(ATR):c.3582-302T>C rs79841072 0.04293
NM_001184.4(ATR):c.5381-41C>T rs34502778 0.04288
NM_001184.4(ATR):c.7655+169A>C rs74775064 0.04282
NM_001184.4(ATR):c.1171-58A>C rs114801305 0.04054
NM_001184.4(ATR):c.3725+18A>G rs73864554 0.03416
NM_001184.4(ATR):c.6687+262A>G rs79174289 0.03041
NM_001184.4(ATR):c.3946-277A>T rs74882709 0.03040
NM_001184.4(ATR):c.2342-51A>G rs75131857 0.02176
NM_001184.4(ATR):c.4266+120A>T rs79992910 0.01901
NM_001184.4(ATR):c.7656-335G>A rs7634495 0.01899
NM_001184.4(ATR):c.1326A>G (p.Lys442=) rs28897765 0.01766
NM_001184.4(ATR):c.946G>A (p.Val316Ile) rs28897764 0.01744
NM_001184.4(ATR):c.1950G>A (p.Glu650=) rs28910270 0.01739
NM_001184.4(ATR):c.2341+311G>A rs7639724 0.01716
NM_001184.4(ATR):c.2875G>A (p.Val959Met) rs28910271 0.01643
NM_001184.4(ATR):c.293-20C>T rs115097590 0.01504
NM_001184.4(ATR):c.4835A>G (p.Asn1612Ser) rs55894265 0.01275
NM_001184.4(ATR):c.7300C>G (p.Pro2434Ala) rs33972295 0.01261
NM_001184.4(ATR):c.891G>C (p.Lys297Asn) rs2229033 0.01036
NM_001184.4(ATR):c.4002G>A (p.Gln1334=) rs56026468 0.01034
NM_001184.4(ATR):c.5868C>T (p.Tyr1956=) rs112018640 0.01020
NM_001184.4(ATR):c.6339A>G (p.Val2113=) rs7635479 0.00964
NM_001184.4(ATR):c.268C>T (p.His90Tyr) rs28897763 0.00813
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.2290A>G (p.Lys764Glu) rs77208665 0.00340
NM_001184.4(ATR):c.1733-213_1733-211del rs140110595
NM_001184.4(ATR):c.1885+39_1885+42del rs764936051
NM_001184.4(ATR):c.1885+43CTAT[7] rs780538224
NM_001184.4(ATR):c.1885+65ATTT[10] rs56661838
NM_001184.4(ATR):c.1885+65ATTT[7] rs56661838
NM_001184.4(ATR):c.1885+65ATTT[8] rs56661838
NM_001184.4(ATR):c.2634-59GT[13] rs56873611
NM_001184.4(ATR):c.2634-61_2634-58del rs1172629064
NM_001184.4(ATR):c.3120G>A (p.Leu1040=) rs28910272
NM_001184.4(ATR):c.3581+39del rs201551475
NM_001184.4(ATR):c.4852+21C>T rs587783332
NM_001184.4(ATR):c.4852+22_4852+23dup rs74269486
NM_001184.4(ATR):c.4852+22dup rs74269486
NM_001184.4(ATR):c.4852+39del rs74269486
NM_001184.4(ATR):c.5739-14_5739-6delinsT rs886058054
NM_001184.4(ATR):c.5898+190C>G rs111896467
NM_001184.4(ATR):c.5898+82A>T rs73864545
NM_001184.4(ATR):c.5898+82_5898+83insAT rs1553758609

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