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Items: 31

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BARD1
Single nucleotide variant
(3 prime UTR variant +1 more)
Breast and/or ovarian cancer
GUncertain significance
BARD1
(S761N +4 more)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+5 more
GConflicting classifications of pathogenicity
BARD1
(R751Q +4 more)
Single nucleotide variant
(missense variant +1 more)
Breast and/or ovarian cancer
+3 more
GUncertain significance
BARD1
(R731G +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+6 more
GConflicting classifications of pathogenicity
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Breast and/or ovarian cancer
+3 more
GLikely benign
BARD1
Single nucleotide variant
(intron variant)
not specified
+3 more
GBenign/Likely benign
BARD1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+5 more
GConflicting classifications of pathogenicity
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Breast and/or ovarian cancer
+1 more
GLikely benign
BARD1
(N626S +3 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
BARD1
(D612V +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+4 more
GConflicting classifications of pathogenicity
BARD1
(T598N +3 more)
Single nucleotide variant
(missense variant +2 more)
not specified
+4 more
GUncertain significance
BARD1
(E580K +3 more)
Single nucleotide variant
(missense variant +2 more)
Breast and/or ovarian cancer
+5 more
GBenign
BARD1
Single nucleotide variant
(intron variant)
Breast and/or ovarian cancer
+2 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +2 more)
BARD1-related disorder
+5 more
GConflicting classifications of pathogenicity
BARD1
(S339N +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
+4 more
GConflicting classifications of pathogenicity
BARD1
(L295S +1 more)
Single nucleotide variant
(missense variant +2 more)
Breast and/or ovarian cancer
+1 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +2 more)
Familial cancer of breast
+4 more
GConflicting classifications of pathogenicity
BARD1
(L239Q +1 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
BARD1
(E223G +1 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
BARD1
(K207R +1 more)
Single nucleotide variant
(missense variant +2 more)
Breast and/or ovarian cancer
+4 more
GBenign/Likely benign
BARD1
(D190N +1 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
BARD1
(I150V +1 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +2 more)
Familial cancer of breast
+3 more
GLikely benign
BARD1
Single nucleotide variant
(intron variant)
Familial cancer of breast
+3 more
GConflicting classifications of pathogenicity
BARD1
(T54S)
Single nucleotide variant
(missense variant +2 more)
Familial cancer of breast
+3 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +2 more)
Breast and/or ovarian cancer
+4 more
GConflicting classifications of pathogenicity
BARD1
(C53G)
Single nucleotide variant
(missense variant +1 more)
Breast and/or ovarian cancer
+3 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+3 more
GConflicting classifications of pathogenicity
BARD1
(R43S)
Single nucleotide variant
(missense variant +1 more)
Breast and/or ovarian cancer
+4 more
GUncertain significance
BARD1
Single nucleotide variant
(synonymous variant +1 more)
Familial cancer of breast
+1 more
GLikely benign
BARD1
(Q11H)
Single nucleotide variant
(missense variant +1 more)
Familial cancer of breast
+4 more
GConflicting classifications of pathogenicity
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