ClinVar Miner

List of variants in gene PDHX reported as benign for X-linked disease

Included ClinVar conditions (311):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_001135024.1(PDHX):c.115+41C>T rs112032820
NM_001135024.1(PDHX):c.115+41_115+43del rs371074122
NM_001135024.1(PDHX):c.115+46G>C rs375130125
NM_001135024.1(PDHX):c.115+82C>A rs2956110
NM_001166158.1(PDHX):c.-202A>G rs113073242
NM_003477.3(PDHX):c.*123A>G rs59918794
NM_003477.3(PDHX):c.*173G>A rs75863418
NM_003477.3(PDHX):c.*200T>C rs16926653
NM_003477.3(PDHX):c.*27A>C rs74524673
NM_003477.3(PDHX):c.*486G>T rs9326
NM_003477.3(PDHX):c.*644C>A rs7808
NM_003477.3(PDHX):c.*890T>C rs1049333
NM_003477.3(PDHX):c.-23C>A rs201033364
NM_003477.3(PDHX):c.-4C>G rs3818401
NM_003477.3(PDHX):c.108T>C (p.Ser36=) rs1049307
NM_003477.3(PDHX):c.1188A>G (p.Leu396=) rs200434738
NM_003477.3(PDHX):c.1331G>A (p.Arg444Lys) rs34398018
NM_003477.3(PDHX):c.241+3G>A rs78878052
NM_003477.3(PDHX):c.301A>G (p.Thr101Ala) rs11539202
NM_003477.3(PDHX):c.339C>T (p.Ile113=) rs34582941
NM_003477.3(PDHX):c.438C>T (p.Asp146=) rs75182779
NM_003477.3(PDHX):c.507C>T (p.Ile169=) rs79170416
NM_003477.3(PDHX):c.531C>T (p.Pro177=) rs76486106
NM_003477.3(PDHX):c.63C>T (p.Pro21=) rs2956109
NM_003477.3(PDHX):c.641+4T>C rs2767035
NM_003477.3(PDHX):c.67C>T (p.Arg23Cys) rs1049306
NM_003477.3(PDHX):c.70C>G (p.Arg24Gly) rs11539201
NM_003477.3(PDHX):c.798T>C (p.Pro266=) rs61760973
NM_003477.3(PDHX):c.858T>C (p.Val286=) rs497582
NM_003477.3(PDHX):c.957G>A (p.Leu319=) rs36047324
NM_003477.3(PDHX):c.976G>C (p.Val326Leu) rs35560997

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