ClinVar Miner

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

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Gene type:
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Total variants: 25
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HGVS dbSNP
NM_001184.4(ATR):c.1350-3T>C rs587783323
NM_001184.4(ATR):c.1626A>G (p.Lys542=) rs762125386
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.2290A>G (p.Lys764Glu) rs77208665
NM_001184.4(ATR):c.2688G>A (p.Leu896=) rs117926957
NM_001184.4(ATR):c.2776T>C (p.Phe926Leu) rs141783863
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.3799G>A (p.Val1267Ile) rs377689383
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.4576A>G (p.Ile1526Val) rs34124242
NM_001184.4(ATR):c.4641+15C>T rs200619976
NM_001184.4(ATR):c.4677C>T (p.Asp1559=) rs112726878
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.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.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.7725G>A (p.Ala2575=) rs587783340
NM_001184.4(ATR):c.992A>G (p.Asp331Gly) rs150008448

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