ClinVar Miner

List of variants in gene AGXT reported as uncertain significance by Counsyl

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Total variants: 10
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HGVS dbSNP
NM_000030.2(AGXT):c.*39G>A rs369979466
NM_000030.2(AGXT):c.1072-91G>A rs180177159
NM_000030.2(AGXT):c.145A>C (p.Met49Leu) rs74205173
NM_000030.2(AGXT):c.260_271del12 (p.Glu87_Leu90del) rs1553648333
NM_000030.2(AGXT):c.423G>C (p.Glu141Asp) rs180177217
NM_000030.2(AGXT):c.686_688dup (p.Lys229_Met230insLys) rs1553648979
NM_000030.2(AGXT):c.781C>G (p.His261Asp) rs778567956
NM_000030.2(AGXT):c.82C>T (p.Pro28Ser) rs376684240
NM_000030.2(AGXT):c.865C>T (p.Arg289Cys) rs180177290
NM_000030.2(AGXT):c.866G>A (p.Arg289His) rs61729604

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