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Items: 44

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEBPA
(K352R +3 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CEBPA
(G340S +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(T337S +3 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
CEBPA
(N188Y +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(Q305R +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(S277L +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(K276R +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
+1 more
GUncertain significance
CEBPA
(G268V +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(A146V +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(A140G +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(S132C +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(S132G +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(G242S +3 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
CEBPA
(A121V +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(P237T +3 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
CEBPA
(T202A +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(A185L +3 more)
Indel
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(H181Y +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(L178V +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
+2 more
GUncertain significance
CEBPA
(A176V +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
Deletion
(inframe deletion)
Acute myeloid leukemia
GUncertain significance
CEBPA
(L144R +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(G137R +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(Y133C +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(G141C +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(G130S +3 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
CEBPA
(P129S +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
+1 more
GUncertain significance
CEBPA
(P128S +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CEBPA
(G158E +3 more)
Single nucleotide variant
(missense variant)
Acute myeloid leukemia
GUncertain significance
CEBPA
(G122R +3 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
CEBPA
(A104T +2 more)
Single nucleotide variant
(missense variant +1 more)
Acute myeloid leukemia
GUncertain significance
CEBPA
(P109S +2 more)
Single nucleotide variant
(missense variant +1 more)
Acute myeloid leukemia
GUncertain significance
CEBPA
(G104S +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Acute myeloid leukemia
GUncertain significance
CEBPA
(G102S +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+2 more
GUncertain significance
CEBPA
(E124del +2 more)
Deletion
(5 prime UTR variant +1 more)
Acute myeloid leukemia
GUncertain significance
CEBPA
(H84Q +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Acute myeloid leukemia
GUncertain significance
CEBPA
(F82L +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
+1 more
GUncertain significance
CEBPA
(A114G +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Acute myeloid leukemia
GUncertain significance
CEBPA
(Y102S +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Acute myeloid leukemia
GUncertain significance
CEBPA
(C42S +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Acute myeloid leukemia
GUncertain significance
CEBPA
(P20T +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Acute myeloid leukemia
+1 more
GUncertain significance
CEBPA
(P23T +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CEBPA
(S21R +2 more)
Single nucleotide variant
(missense variant +1 more)
Acute myeloid leukemia
+1 more
GUncertain significance
CEBPA
(Q20H +2 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+1 more
GUncertain significance
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