ClinVar Miner

List of variants in gene AGXT reported as uncertain significance for Primary hyperoxaluria

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Total variants: 15
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HGVS dbSNP
NM_000030.3(AGXT):c.*160G>A rs776483024
NM_000030.3(AGXT):c.*162A>G rs886055844
NM_000030.3(AGXT):c.*19G>A rs143458283
NM_000030.3(AGXT):c.-14G>A rs376396832
NM_000030.3(AGXT):c.1071+12C>T rs375775541
NM_000030.3(AGXT):c.1071+13G>A rs758413374
NM_000030.3(AGXT):c.165+12G>C rs201989825
NM_000030.3(AGXT):c.35A>G (p.Lys12Arg) rs142969817
NM_000030.3(AGXT):c.484G>A (p.Val162Met) rs147497484
NM_000030.3(AGXT):c.489G>A (p.Leu163=) rs147601535
NM_000030.3(AGXT):c.524+3G>A rs886055839
NM_000030.3(AGXT):c.601G>A (p.Asp201Asn) rs886055840
NM_000030.3(AGXT):c.901C>T (p.Arg301Cys) rs886055841
NM_000030.3(AGXT):c.930C>T (p.Phe310=) rs886055842
NM_000030.3(AGXT):c.942+14T>G rs886055843

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