ClinVar Miner

List of variants in gene ATM reported as likely pathogenic for Hereditary cancer-predisposing syndrome

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Gene type:
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Total variants: 76
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HGVS dbSNP
NM_000051.3(ATM):c.-30-1G>T rs869312754
NM_000051.3(ATM):c.103C>T (p.Arg35Ter) rs55861249
NM_000051.3(ATM):c.1065+1G>T rs201089102
NM_000051.3(ATM):c.1066-1G>A rs876660038
NM_000051.3(ATM):c.1066-2A>T rs1555069514
NM_000051.3(ATM):c.1236-2A>G rs80159221
NM_000051.3(ATM):c.1547T>C (p.Leu516Ser) rs786202195
NM_000051.3(ATM):c.1783_1802+91del rs1555072063
NM_000051.3(ATM):c.186-1G>A rs1259911051
NM_000051.3(ATM):c.1899-1G>A rs1555073065
NM_000051.3(ATM):c.2098C>T (p.Gln700Ter) rs786202743
NM_000051.3(ATM):c.2250+2T>C rs1555075037
NM_000051.3(ATM):c.2250G>A (p.Lys750=) rs1137887
NM_000051.3(ATM):c.2251-10T>G rs730881346
NM_000051.3(ATM):c.2251-1G>C rs876659710
NM_000051.3(ATM):c.2376+1G>A rs730881347
NM_000051.3(ATM):c.2376+1G>C rs730881347
NM_000051.3(ATM):c.2377-2A>G rs1057516553
NM_000051.3(ATM):c.2467-2A>C rs1555082050
NM_000051.3(ATM):c.2467-2A>G rs1555082050
NM_000051.3(ATM):c.2638+1delG rs1131691153
NM_000051.3(ATM):c.2638+2T>C rs587779826
NM_000051.3(ATM):c.2639-384A>G rs1131691154
NM_000051.3(ATM):c.2838+1G>T rs1555083469
NM_000051.3(ATM):c.2839-2A>G rs1060501703
NM_000051.3(ATM):c.2839-3_2839delinsGATACTA rs786202148
NM_000051.3(ATM):c.2849T>G (p.Leu950Arg) rs786203054
NM_000051.3(ATM):c.2921+1G>C rs587781558
NM_000051.3(ATM):c.2921+1G>T rs587781558
NM_000051.3(ATM):c.2922-1G>T rs1555084931
NM_000051.3(ATM):c.3078-1G>A rs750663117
NM_000051.3(ATM):c.3284+1G>A rs864622129
NM_000051.3(ATM):c.3284G>A (p.Arg1095Lys) rs587781815
NM_000051.3(ATM):c.331+1G>A rs1555055356
NM_000051.3(ATM):c.332-1G>A rs747855862
NM_000051.3(ATM):c.3402+1G>C rs1565439606
NM_000051.3(ATM):c.3402+2T>C rs876659430
NM_000051.3(ATM):c.3403-1G>A rs1555091120
NM_000051.3(ATM):c.3576+1G>A rs876660621
NM_000051.3(ATM):c.3576+1G>T rs876660621
NM_000051.3(ATM):c.3576G>T (p.Lys1192Asn) rs587776551
NM_000051.3(ATM):c.3577-1G>C rs1057517226
NM_000051.3(ATM):c.3707_3711TTATT[1] (p.Leu1238fs) rs786201675
NM_000051.3(ATM):c.3747-1G>C rs730881364
NM_000051.3(ATM):c.3848T>C (p.Leu1283Pro) rs730881389
NM_000051.3(ATM):c.3993+1G>A rs200196781
NM_000051.3(ATM):c.3994-1G>T rs1057516238
NM_000051.3(ATM):c.3994-2A>C rs587782276
NM_000051.3(ATM):c.3994-2A>G rs587782276
NM_000051.3(ATM):c.4236+1G>T rs876660674
NM_000051.3(ATM):c.4394T>C (p.Leu1465Pro) rs730881391
NM_000051.3(ATM):c.4397_4398delinsCG (p.Arg1466Pro) rs886038217
NM_000051.3(ATM):c.4436+2T>C rs1555097898
NM_000051.3(ATM):c.4611+1delG rs1565461824
NM_000051.3(ATM):c.4612-3_4616delTAGGTATT rs773012957
NM_000051.3(ATM):c.4735C>T (p.Gln1579Ter) rs869312755
NM_000051.3(ATM):c.4776+1G>T rs771117943
NM_000051.3(ATM):c.4776+2T>A rs587781927
NM_000051.3(ATM):c.4776+2_4776+13delTAATAAAAATTT rs762838462
NM_000051.3(ATM):c.4910-2A>T rs1555103156
NM_000051.3(ATM):c.496+1G>A rs876658500
NM_000051.3(ATM):c.496+5G>A rs796051858
NM_000051.3(ATM):c.5177+5G>A rs759373136
NM_000051.3(ATM):c.5228C>T (p.Thr1743Ile) rs587779844
NM_000051.3(ATM):c.5319+1G>A rs876660175
NM_000051.3(ATM):c.5319+2T>C rs1555105842
NM_000051.3(ATM):c.5497-1G>A rs876660245
NM_000051.3(ATM):c.5497-2A>G rs786203796
NM_000051.3(ATM):c.5674+1G>T rs1565482453
NM_000051.3(ATM):c.5762+1G>A rs869312756
NM_000051.3(ATM):c.5762+1G>T rs869312756
NM_000051.3(ATM):c.72+1G>A rs786204088
NM_000051.3(ATM):c.73-1G>A rs1555054043
NM_000051.3(ATM):c.73-3C>G rs1555054039
NM_000051.3(ATM):c.875C>T (p.Pro292Leu) rs747727055
NM_000051.3(ATM):c.901+2T>C rs1218815157

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