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Items: 44

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CARD9
(N524T)
Single nucleotide variant
(missense variant +1 more)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(E523Q)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
CARD9
(R522Q)
Single nucleotide variant
(missense variant +1 more)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GConflicting classifications of pathogenicity
CARD9
(G514R)
Single nucleotide variant
(missense variant +1 more)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(R509G)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
CARD9
(R503C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
CARD9
(S498G)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
CARD9
(G485A)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
CARD9
Single nucleotide variant
(synonymous variant +1 more)
Inborn genetic diseases
+1 more
GLikely benign
CARD9
(R475L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
CARD9
(H469Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CARD9
(F465L)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(G458V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CARD9
(G457S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CARD9
(D446N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CARD9
(P432S)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(T420M)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(R415Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
CARD9
(L413F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CARD9
(C402R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
CARD9
(A392V)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(E387K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CARD9
(R386Q)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(A380V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CARD9
(H368Q)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(E365G)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(R333H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CARD9
(E326Q)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(R317L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CARD9
(R315L)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(R305H)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(E284A)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(R241Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
CARD9
(D222N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CARD9
(E221G)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(R202W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CARD9
(A198T)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(R160H)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(R148W)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
CARD9
(I144V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CARD9
(S138R)
Single nucleotide variant
(missense variant)
Predisposition to invasive fungal disease due to CARD9 deficiency
+1 more
GUncertain significance
CARD9
(L119P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CARD9
(L85F)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
CARD9
(G16D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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