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Items: 36

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PALB2
(Y1183*)
Single nucleotide variant
(nonsense)
PALB2-related disorder
+4 more
GPathogenic/Likely pathogenic
PALB2
(T1099R)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group N
+5 more
GConflicting classifications of pathogenicity
PALB2
(E1083D)
Single nucleotide variant
(missense variant)
Familial cancer of breast
GBenign
PALB2
(E1083K)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GUncertain significance
PALB2
(W1038*)
Single nucleotide variant
(nonsense)
Familial cancer of breast
GPathogenic
PALB2
(G998E)
Single nucleotide variant
(missense variant)
not specified
+7 more
GBenign/Likely benign
PALB2
(V978fs)
Duplication
(frameshift variant)
Familial cancer of breast
+2 more
GPathogenic
PALB2
(I966V)
Single nucleotide variant
(missense variant)
Breast-ovarian cancer, familial, susceptibility to, 5
+6 more
GUncertain significance
PALB2
(E956K)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
PALB2
(S951P)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
PALB2
(L939W)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
PALB2
(V932M)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+7 more
GBenign/Likely benign
PALB2
Single nucleotide variant
(synonymous variant)
Fanconi anemia complementation group N
+5 more
GBenign/Likely benign
PALB2
(C868R)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
PALB2
(R825T)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
PALB2
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign/Likely benign
PALB2
(A712V)
Single nucleotide variant
(missense variant)
not specified
+6 more
GBenign/Likely benign
PALB2
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign/Likely benign
PALB2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+2 more
GLikely benign
PALB2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+6 more
GBenign/Likely benign
PALB2
(H567Y)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
PALB2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+5 more
GBenign/Likely benign
PALB2
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+6 more
GBenign/Likely benign
PALB2
(S417Y)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
PALB2
(L337S)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
PALB2
(Y334C)
Single nucleotide variant
(missense variant)
Hereditary breast ovarian cancer syndrome
+6 more
GConflicting classifications of pathogenicity
PALB2
(I309V)
Single nucleotide variant
(missense variant)
Hereditary breast ovarian cancer syndrome
+6 more
GBenign/Likely benign
PALB2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
PALB2
(L278Q)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GConflicting classifications of pathogenicity
PALB2
(A245V)
Single nucleotide variant
(missense variant)
Breast-ovarian cancer, familial, susceptibility to, 5
+3 more
GConflicting classifications of pathogenicity
PALB2
(P210L)
Single nucleotide variant
(missense variant)
Hereditary breast ovarian cancer syndrome
+6 more
GConflicting classifications of pathogenicity
PALB2
Deletion
(frameshift variant)
not specified
+11 more
GPathogenic
PALB2
(L100F)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
PALB2
(V78A)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
PALB2
Deletion
(intron variant)
Familial cancer of breast
+3 more
GConflicting classifications of pathogenicity
PALB2
(K18R)
Single nucleotide variant
(missense variant)
Hereditary breast ovarian cancer syndrome
+5 more
GConflicting classifications of pathogenicity
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