ClinVar Miner

List of variants in gene ATR reported as uncertain significance for not provided

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Total variants: 14
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HGVS dbSNP
NM_001184.4(ATR):c.1358_1359del (p.His453fs) rs886044646
NM_001184.4(ATR):c.289A>T (p.Ile97Phe) rs138473993
NM_001184.4(ATR):c.305G>T (p.Trp102Leu) rs794727632
NM_001184.4(ATR):c.4351C>T (p.Arg1451Trp) rs148064542
NM_001184.4(ATR):c.4376A>G (p.Asn1459Ser) rs144591613
NM_001184.4(ATR):c.437C>A (p.Thr146Lys) rs368592452
NM_001184.4(ATR):c.4405A>G (p.Thr1469Ala) rs78895258
NM_001184.4(ATR):c.4509A>T (p.Arg1503=) rs398123602
NM_001184.4(ATR):c.4846T>G (p.Ser1616Ala) rs201492267
NM_001184.4(ATR):c.5739-11_5739-4del rs797045404
NM_001184.4(ATR):c.5739-14_5739-7del rs878853001
NM_001184.4(ATR):c.5900G>A (p.Gly1967Asp) rs751198306
NM_001184.4(ATR):c.6394T>G (p.Tyr2132Asp) rs28910273
NM_001184.4(ATR):c.7667C>G (p.Thr2556Ser) rs200490116

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