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Items: 1 to 100 of 1379

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRIP1
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
BRIP1
Single nucleotide variant
(3 prime UTR variant)
not specified
+1 more
GLikely benign
BRIP1
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
(K1249fs)
Deletion
(frameshift variant)
Familial cancer of breast
+2 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
BRIP1
(P1246L)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GConflicting classifications of pathogenicity
BRIP1
(M1244I)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(M1244fs)
Duplication
(frameshift variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(M1244V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
Indel
(missense variant)
not provided
+1 more
GUncertain significance
BRIP1
(G1243C)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+4 more
GLikely benign
BRIP1
(K1235E)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(F1234C)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
BRIP1
(I1231T)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+2 more
GUncertain significance
BRIP1
(I1231V)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+2 more
GUncertain significance
BRIP1
(I1229fs)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Fanconi anemia complementation group J
+3 more
GLikely benign
BRIP1
(H1227R)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GUncertain significance
BRIP1
(T1226P)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
BRIP1
(E1222V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(E1222fs)
Duplication
(frameshift variant)
Familial cancer of breast
+3 more
GUncertain significance
BRIP1
(E1220K)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(W1217*)
Single nucleotide variant
(nonsense)
Familial cancer of breast
+5 more
GUncertain significance
BRIP1
(W1217C)
Single nucleotide variant
(missense variant)
Hereditary cancer
+4 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+2 more
GLikely benign
BRIP1
(G1211S)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
BRIP1
(D1208H)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GUncertain significance
BRIP1
(K1205Q)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
(E1202G)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+4 more
GUncertain significance
BRIP1
(I1198T)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
(G1197E)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
BRIP1
(L1195fs)
Indel
(frameshift variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(K1194M)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(T1193K)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group J
+2 more
GUncertain significance
BRIP1
(T1193R)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(I1191T)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group J
+2 more
GConflicting classifications of pathogenicity
BRIP1
(I1191V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+4 more
GConflicting classifications of pathogenicity
BRIP1
(A1187T)
Single nucleotide variant
(missense variant)
not specified
+7 more
GConflicting classifications of pathogenicity
BRIP1
(K1186E)
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
(R1183T)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Fanconi anemia complementation group J
+2 more
GLikely benign
BRIP1
(A1182T)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+2 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+2 more
GLikely benign
BRIP1
(E1178del)
Microsatellite
(inframe_deletion)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(E1178V)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+2 more
GUncertain significance
BRIP1
(K1177E)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BRIP1
Indel
(inframe_insertion)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
(I1176fs)
Duplication
(frameshift variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
BRIP1
(D1169Y)
Single nucleotide variant
(missense variant)
Hereditary breast ovarian cancer syndrome
+4 more
GUncertain significance
BRIP1
(K1168N)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
(A1167T)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group J
+3 more
GUncertain significance
BRIP1
(I1165L)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+3 more
GLikely benign
BRIP1
(A1159T)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
BRIP1
(L1158W)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
(N1156S)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
GLikely benign
BRIP1
(G1155E)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
BRIP1
(R1154fs)
Indel
(frameshift variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
BRIP1
(R1154T)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
not specified
+6 more
GConflicting classifications of pathogenicity
BRIP1
(A1150P)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group J
+3 more
GUncertain significance
BRIP1
(D1148E)
Single nucleotide variant
(missense variant)
not specified
+6 more
GConflicting classifications of pathogenicity
BRIP1
(N1147K)
Single nucleotide variant
(missense variant)
Fanconi anemia complementation group J
+2 more
GUncertain significance
BRIP1
(N1147fs)
Duplication
(frameshift variant)
Fanconi anemia complementation group J
+3 more
GConflicting classifications of pathogenicity
BRIP1
(E1145K)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
(E1144G)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+4 more
GConflicting classifications of pathogenicity
BRIP1
(D1141G)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
(D1141A)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+2 more
GUncertain significance
BRIP1
(P1139L)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
BRIP1
(D1138V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
(D1138Y)
Indel
(missense variant)
not specified
+4 more
GUncertain significance
BRIP1
(D1138N)
Inversion
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+6 more
GBenign
BRIP1
(L1136F)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+2 more
GUncertain significance
BRIP1
(E1135Q)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
(P1134fs)
Deletion
(frameshift variant)
not provided
+3 more
GConflicting classifications of pathogenicity
BRIP1
(F1132L)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
BRIP1
(Y1131fs)
Microsatellite
(frameshift variant)
Fanconi anemia complementation group J
+5 more
GLikely pathogenic
BRIP1
(I1130T)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+4 more
GUncertain significance
BRIP1
(I1130V)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GUncertain significance
BRIP1
(E1128Q)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BRIP1
Single nucleotide variant
(synonymous variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
BRIP1
Single nucleotide variant
(synonymous variant)
Familial cancer of breast
+2 more
GLikely benign
BRIP1
(E1126D)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+6 more
GConflicting classifications of pathogenicity
BRIP1
(A1125del)
Deletion
(inframe_deletion)
Breast and/or ovarian cancer
+5 more
GUncertain significance
BRIP1
(E1124fs)
Deletion
(frameshift variant)
Hereditary cancer-predisposing syndrome
+3 more
GLikely pathogenic
BRIP1
(E1124G)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+3 more
GUncertain significance
BRIP1
(T1123A)
Single nucleotide variant
(missense variant)
Familial cancer of breast
+4 more
GUncertain significance
BRIP1
Deletion
(nonsense)
Hereditary cancer-predisposing syndrome
GLikely pathogenic
BRIP1
(R1119K)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
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