ClinVar Miner

List of variants in gene AGMAT studied for not specified

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_024758.5(AGMAT):c.592A>C (p.Lys198Gln) rs147805030 0.00042
NM_024758.5(AGMAT):c.674G>A (p.Arg225Gln) rs200508005 0.00024
NM_024758.5(AGMAT):c.290T>C (p.Ile97Thr) rs148899500 0.00007
NM_024758.5(AGMAT):c.284G>A (p.Arg95His) rs549021034 0.00005
NM_024758.5(AGMAT):c.341T>C (p.Leu114Pro) rs772742125 0.00004
NM_024758.5(AGMAT):c.595C>A (p.Leu199Ile) rs370906598 0.00003
NM_024758.5(AGMAT):c.953T>C (p.Leu318Pro) rs574567828 0.00003
NM_024758.5(AGMAT):c.1004C>T (p.Ala335Val) rs202068651 0.00002
NM_024758.5(AGMAT):c.802G>C (p.Gly268Arg) rs1449683297 0.00002
NM_024758.5(AGMAT):c.406G>A (p.Asp136Asn) rs750427999 0.00001
NM_024758.5(AGMAT):c.574G>A (p.Asp192Asn) rs749470775 0.00001
NM_024758.5(AGMAT):c.727C>T (p.Arg243Trp) rs138227623 0.00001
NM_024758.5(AGMAT):c.944G>A (p.Gly315Asp) rs1248694641 0.00001
NM_024758.5(AGMAT):c.277G>A (p.Gly93Arg) rs2521792140
NM_024758.5(AGMAT):c.292C>T (p.Arg98Trp)
NM_024758.5(AGMAT):c.346T>G (p.Phe116Val)
NM_024758.5(AGMAT):c.510A>T (p.Gln170His)
NM_024758.5(AGMAT):c.557C>T (p.Ala186Val)
NM_024758.5(AGMAT):c.563C>T (p.Thr188Met)
NM_024758.5(AGMAT):c.604G>A (p.Gly202Arg)
NM_024758.5(AGMAT):c.620G>A (p.Arg207Gln) rs201546181
NM_024758.5(AGMAT):c.653G>A (p.Arg218His)
NM_024758.5(AGMAT):c.764T>C (p.Leu255Pro)
NM_024758.5(AGMAT):c.817A>G (p.Ile273Val)
NM_024758.5(AGMAT):c.971C>A (p.Pro324Gln) rs749080126
NM_024758.5(AGMAT):c.980T>C (p.Leu327Pro) rs2521754655

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