ClinVar Miner

List of variants in gene ATR reported as likely benign for Hereditary cancer-predisposing syndrome

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Total variants: 25
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HGVS dbSNP
NM_001184.4(ATR):c.2079-28T>C rs767195127
NM_001184.4(ATR):c.2533-17T>C rs869312489
NM_001184.4(ATR):c.292+745A>C rs78050501
NM_001184.4(ATR):c.3172-266C>A rs143205618
NM_001184.4(ATR):c.3358-1899T>G rs869312482
NM_001184.4(ATR):c.3450+567A>G rs564240158
NM_001184.4(ATR):c.3451-641C>A rs373891058
NM_001184.4(ATR):c.3581+486T>C rs72996190
NM_001184.4(ATR):c.3726-24C>A rs869312487
NM_001184.4(ATR):c.3819+389T>C rs559805028
NM_001184.4(ATR):c.3945+483G>A rs149815404
NM_001184.4(ATR):c.3946-104A>G rs869312483
NM_001184.4(ATR):c.5380+341A>T rs869312490
NM_001184.4(ATR):c.59+1024G>A rs6788362
NM_001184.4(ATR):c.59+3019A>C rs75518582
NM_001184.4(ATR):c.6221+2962T>C rs869312488
NM_001184.4(ATR):c.6553-490C>G rs749552840
NM_001184.4(ATR):c.6687+210T>G rs869312485
NM_001184.4(ATR):c.6898-69G>A rs115906468
NM_001184.4(ATR):c.7192+98A>G rs78659656
NM_001184.4(ATR):c.7761+375C>T rs11717703
NM_001184.4(ATR):c.7762-208T>C rs552872123
NM_001184.4(ATR):c.7762-209G>T rs577916091
NM_001184.4(ATR):c.7762-439T>C rs869312484
NM_001184.4(ATR):c.7762-724C>T rs869312486

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