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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COQ8B
(R477Q +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 9
+1 more
GPathogenic/Likely pathogenic
COQ8B
Single nucleotide variant
(intron variant)
Nephrotic syndrome, type 9
+1 more
GConflicting classifications of pathogenicity
COQ8B
Single nucleotide variant
(splice donor variant)
Nephrotic syndrome, type 9
GPathogenic
COQ8B
(D209H +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 9
GConflicting classifications of pathogenicity
COQ8B
(S205N +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 9
+1 more
GConflicting classifications of pathogenicity
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