ClinVar Miner

List of variants in gene SDHA reported as uncertain significance for Leigh syndrome

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_001294332.1(SDHA):c.-63G>A rs886060513
NM_004168.4(SDHA):c.*133G>C rs193112615
NM_004168.4(SDHA):c.*189C>T rs185107377
NM_004168.4(SDHA):c.*75A>G rs886060517
NM_004168.4(SDHA):c.-1C>T rs560932680
NM_004168.4(SDHA):c.1055G>A (p.Arg352Gln) rs199844384
NM_004168.4(SDHA):c.1092C>T (p.Val364=) rs886060515
NM_004168.4(SDHA):c.1150T>G (p.Ser384Ala) rs776888362
NM_004168.4(SDHA):c.133G>A (p.Ala45Thr) rs140736646
NM_004168.4(SDHA):c.1462G>A (p.Ala488Thr) rs369100772
NM_004168.4(SDHA):c.155C>T (p.Ser52Phe) rs377470390
NM_004168.4(SDHA):c.1580G>A (p.Arg527His) rs766352407
NM_004168.4(SDHA):c.1660C>T (p.Arg554Trp) rs9809219
NM_004168.4(SDHA):c.1753C>T (p.Arg585Trp) rs200397144
NM_004168.4(SDHA):c.1794+105dup rs1561011159
NM_004168.4(SDHA):c.1909-12_1909-11del rs372662724
NM_004168.4(SDHA):c.1919A>G (p.Glu640Gly) rs372480044
NM_004168.4(SDHA):c.1973C>T (p.Pro658Leu) rs377632619
NM_004168.4(SDHA):c.269T>C (p.Val90Ala) rs886060514
NM_004168.4(SDHA):c.441C>T (p.Pro147=) rs201453889
NM_004168.4(SDHA):c.442G>A (p.Ala148Thr) rs375576259
NM_004168.4(SDHA):c.445G>A (p.Ala149Thr) rs575617625
NM_004168.4(SDHA):c.448G>A (p.Val150Met) rs542980860
NM_004168.4(SDHA):c.613T>C (p.Tyr205His) rs61754481
NM_004168.4(SDHA):c.694C>T (p.Arg232Cys) rs878854635
NM_004168.4(SDHA):c.704T>C (p.Ile235Thr) rs144513891
NM_004168.4(SDHA):c.723C>T (p.Asp241=) rs146653693
NM_004168.4(SDHA):c.739A>G (p.Ile247Val) rs571292356
NM_004168.4(SDHA):c.812C>G (p.Thr271Ser) rs765611464
NM_004168.4(SDHA):c.830C>T (p.Thr277Met) rs367721665
NM_004168.4(SDHA):c.902A>G (p.Tyr301Cys)
NM_004168.4(SDHA):c.92G>A (p.Arg31Gln) rs752532780
NM_004168.4(SDHA):c.955A>C (p.Ile319Leu) rs377509915
NM_004168.4(SDHA):c.991G>A (p.Ala331Thr) rs200526913
NM_004168.4(SDHA):c.994C>T (p.Pro332Ser) rs373509391

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