ClinVar Miner

List of variants in gene NDUFS8 reported as pathogenic for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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NM_002496.4(NDUFS8):c.187G>C (p.Glu63Gln) rs397514618
NM_002496.4(NDUFS8):c.229C>T (p.Arg77Trp) rs146766138
NM_002496.4(NDUFS8):c.236C>T (p.Pro79Leu) rs28939679
NM_002496.4(NDUFS8):c.254C>T (p.Pro85Leu) rs121912639
NM_002496.4(NDUFS8):c.305G>A (p.Arg102His) rs121912638
NM_002496.4(NDUFS8):c.413G>A (p.Arg138His) rs111033588
NM_002496.4(NDUFS8):c.476C>A (p.Ala159Asp) rs397514617

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