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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BAP1
Single nucleotide variant
(intron variant)
not specified
+5 more
GBenign/Likely benign
BAP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
BAP1
Single nucleotide variant
(synonymous variant)
BAP1-related condition
+3 more
GConflicting classifications of pathogenicity
BAP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
BAP1
(A321T)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
BAP1
Single nucleotide variant
(synonymous variant)
BAP1-related condition
+3 more
GConflicting classifications of pathogenicity
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