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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEBPA
(G242S +3 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
CEBPA
(P239A +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
+2 more
GUncertain significance
CEBPA
(P237T +3 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
CEBPA
(G223S +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
+3 more
GConflicting classifications of pathogenicity
CEBPA
(P139R +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(G122E +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CEBPA
(G122R +3 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
CEBPA
(S21R +2 more)
Single nucleotide variant
(missense variant +1 more)
Acute myeloid leukemia
+1 more
GUncertain significance
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