ClinVar Miner

List of variants in gene NDUFS6 reported as uncertain significance for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_004553.5(NDUFS6):c.*15C>T rs200445799
NM_004553.5(NDUFS6):c.*27A>G rs370587409
NM_004553.5(NDUFS6):c.155G>C (p.Arg52Thr) rs768060274
NM_004553.5(NDUFS6):c.198C>T (p.Asn66=) rs140887831
NM_004553.5(NDUFS6):c.24C>T (p.Cys8=) rs886060511
NM_004553.5(NDUFS6):c.25C>T (p.Arg9Trp) rs376509886
NM_004553.5(NDUFS6):c.27G>C (p.Arg9=) rs886060512
NM_004553.5(NDUFS6):c.369C>T (p.His123=) rs745565855
NM_004553.6(NDUFS6):c.*46C>T
NM_004553.6(NDUFS6):c.*99G>C
NM_004553.6(NDUFS6):c.31C>G (p.Leu11Val) rs755222875

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