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Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PALB2
(Y1183*)
Single nucleotide variant
(nonsense)
Hereditary cancer-predisposing syndrome
+4 more
GPathogenic/Likely pathogenic
PALB2
(G998E)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GBenign/Likely benign
PALB2
(S951P)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
PALB2
(C949Y)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+2 more
GConflicting classifications of pathogenicity
PALB2
(V932M)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GBenign/Likely benign
PALB2
(P864S)
Single nucleotide variant
(missense variant)
not specified
+7 more
GBenign/Likely benign
PALB2
(E837K)
Single nucleotide variant
(missense variant)
not specified
+6 more
GConflicting classifications of pathogenicity
PALB2
(K819R)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
PALB2
(R753Q)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
PALB2
(E672Q)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GBenign
PALB2
(E669fs)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic
PALB2
Deletion
(inframe_deletion)
Fanconi anemia complementation group N
+5 more
GUncertain significance
PALB2
(Q559R)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group N
+7 more
GBenign/Likely benign
PALB2
(L337S)
Single nucleotide variant
(missense variant)
not specified
+5 more
GConflicting classifications of pathogenicity
PALB2
(I309V)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group N
+6 more
GBenign/Likely benign
PALB2
(T300I)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GConflicting classifications of pathogenicity
PALB2
(L278H)
Indel
(missense variant)
not provided
+7 more
GConflicting classifications of pathogenicity
PALB2
(N241D)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GBenign
PALB2
(P210L)
Single nucleotide variant
(missense variant)
not provided
+6 more
GConflicting classifications of pathogenicity
PALB2
(P65L)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
PALB2
(L32V)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+4 more
GConflicting classifications of pathogenicity
PALB2
(K18R)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
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