ClinVar Miner

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

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Total variants: 15
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HGVS dbSNP
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.2242A>G (p.Thr748Ala) rs879255363
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.3945+2dup rs537031994
NM_001184.4(ATR):c.4576A>G (p.Ile1526Val) rs34124242
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.5739-11_5739-4del rs797045404
NM_001184.4(ATR):c.7041+8G>A rs201106004
NM_001184.4(ATR):c.992A>G (p.Asp331Gly) rs150008448

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