ClinVar Miner

List of variants in gene SDHA reported as pathogenic for adrenal gland disease

Included ClinVar conditions (124):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_004168.4(SDHA):c.1054C>T (p.Arg352Ter) rs746165168
NM_004168.4(SDHA):c.1151C>G (p.Ser384Ter) rs151170408
NM_004168.4(SDHA):c.1258C>T (p.Gln420Ter)
NM_004168.4(SDHA):c.1468G>T (p.Glu490Ter) rs1554000360
NM_004168.4(SDHA):c.1471G>T (p.Glu491Ter) rs778207102
NM_004168.4(SDHA):c.1526_1527delinsGA (p.Ser509Ter) rs1064793567
NM_004168.4(SDHA):c.1534C>T (p.Arg512Ter) rs748089700
NM_004168.4(SDHA):c.1547dup (p.Lys517fs) rs1554000378
NM_004168.4(SDHA):c.1579del (p.Arg527fs)
NM_004168.4(SDHA):c.1615dup (p.Ile539fs) rs1554001843
NM_004168.4(SDHA):c.1629T>G (p.Tyr543Ter) rs747249998
NM_004168.4(SDHA):c.1753C>T (p.Arg585Trp) rs200397144
NM_004168.4(SDHA):c.1765C>T (p.Arg589Trp) rs387906780
NM_004168.4(SDHA):c.1A>G (p.Met1Val) rs1061517
NM_004168.4(SDHA):c.223C>T (p.Arg75Ter) rs781764920
NM_004168.4(SDHA):c.253_256dup (p.Asn86delinsIleTer) rs1560986132
NM_004168.4(SDHA):c.28del (p.Leu10fs)
NM_004168.4(SDHA):c.378del (p.Thr126_Val127insTer) rs1553997617
NM_004168.4(SDHA):c.46_52dup (p.Leu18fs) rs1560980939
NM_004168.4(SDHA):c.508C>T (p.Gln170Ter)
NM_004168.4(SDHA):c.553C>T (p.Gln185Ter) rs775827529
NM_004168.4(SDHA):c.5C>A (p.Ser2Ter)
NM_004168.4(SDHA):c.615T>A (p.Tyr205Ter) rs876658486
NM_004168.4(SDHA):c.619_620delinsC (p.Ser208fs)
NM_004168.4(SDHA):c.628C>T (p.Arg210Ter) rs775143272
NM_004168.4(SDHA):c.644_645del (p.Tyr215fs) rs1560989804
NM_004168.4(SDHA):c.667del (p.Asp223fs) rs587782077
NM_004168.4(SDHA):c.688del (p.Glu230fs) rs1553998199
NM_004168.4(SDHA):c.722_726del (p.Asp241fs) rs1553998229
NM_004168.4(SDHA):c.762_770+17del rs1041809852
NM_004168.4(SDHA):c.775del (p.Tyr259fs) rs1553998606
NM_004168.4(SDHA):c.880C>T (p.Gln294Ter) rs1560992565
NM_004168.4(SDHA):c.897_1260+1del
NM_004168.4(SDHA):c.91C>T (p.Arg31Ter) rs142441643
NM_004168.4(SDHA):c.942_945delinsTCC (p.Glu314fs)
NM_004168.4(SDHA):c.985C>T (p.Arg329Ter) rs771328239
NM_004168.4(SDHA):c.995_996del (p.Pro332fs) rs1560994766

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