U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 79

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRIP1
(I1191V)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+6 more
GConflicting classifications of pathogenicity
BRIP1
(A1187T)
Single nucleotide variant
(missense variant)
not provided
+7 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
BRIP1
(D1148E)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
BRIP1
(D1138Y)
Indel
(missense variant)
not specified
+4 more
GUncertain significance
BRIP1
(A1125del)
Deletion
(inframe_deletion)
Breast and/or ovarian cancer
+5 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GLikely benign
BRIP1
(C1067S)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GUncertain significance
BRIP1
(R1035C)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+7 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+5 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+6 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
BRIP1
(Q944E)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+8 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GConflicting classifications of pathogenicity
BRIP1
(V935G)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+7 more
GConflicting classifications of pathogenicity
BRIP1
(D904N)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
BRIP1
(I896V)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+4 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
BRIP1
(R848G)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GUncertain significance
BRIP1
(R814C)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+7 more
GConflicting classifications of pathogenicity
BRIP1
(R798*)
Single nucleotide variant
(nonsense)
Breast and/or ovarian cancer
+9 more
GPathogenic/Likely pathogenic
BRIP1
(N775S)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+7 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+4 more
GLikely benign
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+6 more
GBenign/Likely benign
BRIP1
(R762H)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
BRIP1
Single nucleotide variant
(intron variant)
not specified
+6 more
GBenign/Likely benign
BRIP1
(Y748*)
Single nucleotide variant
(nonsense)
Breast and/or ovarian cancer
+5 more
GPathogenic/Likely pathogenic
BRIP1
(I746V)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+6 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(synonymous variant)
not provided
+6 more
GBenign/Likely benign
BRIP1
(Q740H)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+8 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(intron variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
BRIP1
(P696L)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GUncertain significance
BRIP1
(T686A)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
BRIP1
(E671fs)
Deletion
(frameshift variant)
Breast and/or ovarian cancer
GLikely pathogenic
BRIP1
(R658G)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+3 more
GLikely benign
BRIP1
Microsatellite
(intron variant)
Breast and/or ovarian cancer
+4 more
GConflicting classifications of pathogenicity
BRIP1
(R581Q)
Single nucleotide variant
(missense variant)
not provided
+5 more
GUncertain significance
BRIP1
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
BRIP1
(S542R)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Breast and/or ovarian cancer
+3 more
GLikely benign
BRIP1
(L477S)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(R459S)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+3 more
GUncertain significance
BRIP1
(R419W)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+8 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Fanconi anemia complementation group J
+5 more
GLikely benign
BRIP1
Deletion
(intron variant)
Hereditary breast ovarian cancer syndrome
+4 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Fanconi anemia complementation group J
+4 more
GBenign/Likely benign
BRIP1
(A349T)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+4 more
GUncertain significance
BRIP1
(L347P)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+5 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
not provided
+5 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(intron variant)
Familial cancer of breast
+7 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(splice donor variant)
Fanconi anemia complementation group J
+4 more
GPathogenic/Likely pathogenic
BRIP1
(K297R)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
BRIP1
(P286S)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+3 more
GUncertain significance
BRIP1
(I275V)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+5 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Breast and/or ovarian cancer
+3 more
GLikely benign
BRIP1
(T266M)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+7 more
GUncertain significance
BRIP1
(R264W)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+7 more
GConflicting classifications of pathogenicity
BRIP1
(T260A)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+6 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Fanconi anemia complementation group J
+7 more
GBenign/Likely benign
BRIP1
(C219R)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+5 more
GUncertain significance
BRIP1
(H213fs)
Deletion
(frameshift variant)
Breast and/or ovarian cancer
+2 more
GPathogenic/Likely pathogenic
BRIP1
(S197F)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+5 more
GUncertain significance
BRIP1
(N196S)
Single nucleotide variant
(missense variant)
not specified
+7 more
GConflicting classifications of pathogenicity
BRIP1
(L195P)
Single nucleotide variant
(missense variant)
Neoplasm of ovary
+7 more
GBenign/Likely benign
BRIP1
(V193I)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+7 more
GBenign/Likely benign
BRIP1
(R173H)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
BRIP1
(R173C)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
BRIP1
(L138S)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GUncertain significance
BRIP1
(T133A)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+3 more
GUncertain significance
BRIP1
Duplication
(intron variant)
Familial cancer of breast
+5 more
GBenign/Likely benign
BRIP1
Single nucleotide variant
(intron variant)
Breast and/or ovarian cancer
+5 more
GConflicting classifications of pathogenicity
BRIP1
(R106H)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+8 more
GConflicting classifications of pathogenicity
BRIP1
Deletion
(inframe_deletion)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
BRIP1
(S85L)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GUncertain significance
BRIP1
(P47A)
Single nucleotide variant
(missense variant)
Breast and/or ovarian cancer
+7 more
GConflicting classifications of pathogenicity
BRIP1
(E45*)
Single nucleotide variant
(nonsense)
Breast and/or ovarian cancer
+5 more
GPathogenic/Likely pathogenic
BRIP1
Single nucleotide variant
(intron variant)
Familial cancer of breast
+6 more
GBenign
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
Format
Items per page
Sort by
Choose Destination