ClinVar Miner

List of variants reported as likely benign for Mitochondrial complex II deficiency; Paragangliomas 5

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Total variants: 25
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HGVS dbSNP
NM_004168.4(SDHA):c.-7A>C rs751633537
NM_004168.4(SDHA):c.1026G>A (p.Val342=) rs1060505004
NM_004168.4(SDHA):c.1071T>C (p.Cys357=) rs1553999410
NM_004168.4(SDHA):c.1140G>A (p.Leu380=) rs146348714
NM_004168.4(SDHA):c.1261-4A>T rs1553999703
NM_004168.4(SDHA):c.1305G>C (p.Leu435=) rs35964044
NM_004168.4(SDHA):c.1422A>G (p.Ser474=) rs201868424
NM_004168.4(SDHA):c.1443C>A (p.Val481=) rs751871185
NM_004168.4(SDHA):c.1476T>C (p.Ser492=) rs1376968004
NM_004168.4(SDHA):c.150+9A>G rs1553997201
NM_004168.4(SDHA):c.1572C>G (p.Ala524=) rs185679709
NM_004168.4(SDHA):c.1599A>G (p.Gln533=) rs1407806818
NM_004168.4(SDHA):c.1614A>G (p.Lys538=) rs1554001847
NM_004168.4(SDHA):c.1664-4C>G rs774876028
NM_004168.4(SDHA):c.1794+8T>G rs1050394308
NM_004168.4(SDHA):c.1806T>C (p.Asp602=) rs1554002427
NM_004168.4(SDHA):c.1857G>A (p.Glu619=) rs1247081812
NM_004168.4(SDHA):c.1926A>G (p.Arg642=) rs1554002873
NM_004168.4(SDHA):c.1989C>T (p.Ser663=) rs1554002913
NM_004168.4(SDHA):c.390C>T (p.Ser130=) rs748976493
NM_004168.4(SDHA):c.627G>A (p.Leu209=) rs149821224
NM_004168.4(SDHA):c.64-10G>A rs1553997159
NM_004168.4(SDHA):c.789C>T (p.Tyr263=) rs1553998616
NM_004168.4(SDHA):c.822C>A (p.Gly274=) rs34771391
NM_004168.4(SDHA):c.942G>A (p.Glu314=) rs1553998977

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