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Items: 31

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRIP1
Insertion
(inframe_insertion)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Fanconi anemia complementation group J
+2 more
GLikely benign
BRIP1
(E1126D)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+6 more
GConflicting classifications of pathogenicity
BRIP1
(S1075L)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+4 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+6 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GConflicting classifications of pathogenicity
BRIP1
(L922*)
Single nucleotide variant
(nonsense)
Neoplasm of ovary
+5 more
GPathogenic/Likely pathogenic
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+6 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+2 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(intron variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+6 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+4 more
GLikely benign
BRIP1
(R419W)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+8 more
GConflicting classifications of pathogenicity
BRIP1
(A349P)
Single nucleotide variant
(missense variant)
BRIP1-related disorder
+6 more
GPathogenic/Likely pathogenic
BRIP1
(K297R)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
BRIP1
(E296Q)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
BRIP1
(R251C)
Single nucleotide variant
(missense variant)
Hereditary breast ovarian cancer syndrome
+4 more
GPathogenic/Likely pathogenic
BRIP1
Single nucleotide variant
(synonymous variant)
Fanconi anemia complementation group J
+7 more
GBenign/Likely benign
BRIP1
(S230L)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+5 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
BRIP1-related disorder
+6 more
GBenign/Likely benign
BRIP1
(S197P)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
BRIP1
(L195P)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+7 more
GBenign/Likely benign
BRIP1
(T178I)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group J
+3 more
GUncertain significance
BRIP1
(R173C)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(splice acceptor variant)
Familial cancer of breast
+4 more
GPathogenic/Likely pathogenic
BRIP1
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
BRIP1
(T124A)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
BRIP1
(T113I)
Single nucleotide variant
(missense variant)
BRIP1-related disorder
+4 more
GUncertain significance
BRIP1
(R106H)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+8 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
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