ClinVar Miner

List of variants in gene SIRT1 reported as uncertain significance for not specified

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Gene type:
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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_012238.5(SIRT1):c.535A>G (p.Arg179Gly) rs200805107 0.00013
NM_012238.5(SIRT1):c.1617T>G (p.Ser539Arg) rs192990424 0.00007
NM_012238.5(SIRT1):c.446G>A (p.Gly149Asp) rs978488168 0.00006
NM_012238.5(SIRT1):c.578T>C (p.Met193Thr) rs200994303 0.00004
NM_012238.5(SIRT1):c.1274C>G (p.Ala425Gly) rs201635394 0.00003
NM_012238.5(SIRT1):c.1993G>A (p.Val665Ile) rs201730062 0.00003
NM_012238.5(SIRT1):c.896T>C (p.Ile299Thr) rs199983221 0.00003
NM_012238.5(SIRT1):c.1289A>G (p.Lys430Arg) rs772640272 0.00001
NM_012238.5(SIRT1):c.1417C>T (p.His473Tyr) rs751498023 0.00001
NM_012238.5(SIRT1):c.1510C>A (p.Pro504Thr) rs116499760 0.00001
NM_012238.5(SIRT1):c.2098A>C (p.Asn700His) rs747251569 0.00001
NM_012238.5(SIRT1):c.475T>C (p.Ser159Pro) rs200660028 0.00001
NM_012238.5(SIRT1):c.580A>G (p.Ile194Val) rs1292146988 0.00001
NM_012238.5(SIRT1):c.1078A>G (p.Ile360Val)
NM_012238.5(SIRT1):c.1195C>T (p.Pro399Ser) rs1047393773
NM_012238.5(SIRT1):c.1246G>C (p.Glu416Gln)
NM_012238.5(SIRT1):c.1255C>A (p.Pro419Thr) rs775426483
NM_012238.5(SIRT1):c.1325C>G (p.Ser442Cys)
NM_012238.5(SIRT1):c.1655T>C (p.Ile552Thr)
NM_012238.5(SIRT1):c.1760A>T (p.Asn587Ile) rs2492964799
NM_012238.5(SIRT1):c.1783A>G (p.Met595Val)
NM_012238.5(SIRT1):c.1936C>A (p.Pro646Thr)
NM_012238.5(SIRT1):c.1958A>G (p.His653Arg)
NM_012238.5(SIRT1):c.1994T>A (p.Val665Asp)
NM_012238.5(SIRT1):c.2030G>A (p.Ser677Asn)
NM_012238.5(SIRT1):c.2065A>G (p.Met689Val)
NM_012238.5(SIRT1):c.2158G>A (p.Asp720Asn) rs2492974840
NM_012238.5(SIRT1):c.436C>G (p.Leu146Val) rs1842500910
NM_012238.5(SIRT1):c.689A>T (p.Glu230Val) rs2492897027
NM_012238.5(SIRT1):c.829G>A (p.Asp277Asn)

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