ClinVar Miner

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

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Gene type:
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Total variants: 68
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HGVS dbSNP
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.1350-3T>C rs587783323
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.1815T>C (p.Asp605=) rs2227929
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.196G>A (p.Val66Met) rs758564083
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.2290A>G (p.Lys764Glu) rs77208665
NM_001184.4(ATR):c.2442A>G (p.Glu814=) rs55895932
NM_001184.4(ATR):c.2637C>T (p.Ala879=) rs150512706
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.2776T>C (p.Phe926Leu) rs141783863
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.3120G>A (p.Leu1040=) rs28910272
NM_001184.4(ATR):c.3172-26T>A rs76852171
NM_001184.4(ATR):c.3424A>G (p.Ser1142Gly) rs149008479
NM_001184.4(ATR):c.3614A>G (p.His1205Arg) rs1553767201
NM_001184.4(ATR):c.3725+18A>G rs73864554
NM_001184.4(ATR):c.3726-47A>G rs73240314
NM_001184.4(ATR):c.3799G>A (p.Val1267Ile) rs377689383
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.4306A>G (p.Asn1436Asp) rs587783328
NM_001184.4(ATR):c.4351C>T (p.Arg1451Trp) rs148064542
NM_001184.4(ATR):c.4383-47A>G rs58348002
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.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.5196+1G>A rs1553760567
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.5305G>C (p.Glu1769Gln) rs376811787
NM_001184.4(ATR):c.5381-41C>T rs34502778
NM_001184.4(ATR):c.5460T>C (p.Tyr1820=) rs2227932
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.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.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.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.7274G>A (p.Arg2425Gln) rs2229032
NM_001184.4(ATR):c.7300C>G (p.Pro2434Ala) rs33972295
NM_001184.4(ATR):c.7725G>A (p.Ala2575=) rs587783340
NM_001184.4(ATR):c.7875G>A (p.Gln2625=) rs1802904
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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