ClinVar Miner

List of variants in gene SDHA reported by Mayo Clinic Laboratories, Mayo Clinic

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Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_004168.4(SDHA):c.1523C>T (p.Thr508Ile) rs151266052 0.00245
NM_004168.4(SDHA):c.133G>A (p.Ala45Thr) rs140736646 0.00058
NM_004168.4(SDHA):c.91C>T (p.Arg31Ter) rs142441643 0.00025
NM_004168.4(SDHA):c.-2A>T rs763680697 0.00022
NM_004168.4(SDHA):c.1979C>G (p.Ala660Gly) rs191412461 0.00013
NM_004168.4(SDHA):c.1591G>A (p.Val531Met) rs371056571 0.00009
NM_004168.4(SDHA):c.1534C>T (p.Arg512Ter) rs748089700 0.00005
NM_004168.4(SDHA):c.1135C>T (p.Arg379Cys) rs749309213 0.00002
NM_004168.4(SDHA):c.1799G>A (p.Arg600Gln) rs1126568 0.00002
NM_004168.4(SDHA):c.583C>T (p.Arg195Trp) rs1337777456 0.00001
NM_004168.4(SDHA):c.835A>G (p.Met279Val) rs755913710 0.00001
NM_004168.4(SDHA):c.1349A>G (p.Asn450Ser) rs1579409723
NM_004168.4(SDHA):c.1886A>G (p.Tyr629Cys) rs6960
NM_004168.4(SDHA):c.1894G>T (p.Val632Phe) rs369639811
NM_004168.4(SDHA):c.321C>G (p.Ile107Met) rs1734953765
NM_004168.4(SDHA):c.338A>T (p.Asn113Ile) rs1734955271
NM_004168.4(SDHA):c.698G>T (p.Gly233Val) rs878854636
NM_004168.4(SDHA):c.872A>T (p.Glu291Val) rs1336029027
NM_004168.4(SDHA):c.994C>T (p.Pro332Ser) rs373509391

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