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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRIP1
(P1134fs)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+6 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(intron variant)
Breast and/or ovarian cancer
+6 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Fanconi anemia complementation group J
+6 more
GBenign/Likely benign
BRIP1
(H285R)
Single nucleotide variant
(missense variant)
Hereditary breast ovarian cancer syndrome
+6 more
GConflicting classifications of pathogenicity
BRIP1
(R173C)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+6 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
BRIP1-related condition
+4 more
GConflicting classifications of pathogenicity
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