Project HERA
BARD1 variants
Every BARD1 variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
BARD1 variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
BARD1
NM_000465.4:c.1285G>A
NP_000456.2:p.(E429K)
VUS
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BARD1
NM_000465.4:c.1935_1954dup
NP_000456.2:p.(E652Vfs*69)
Likely Pathogenic
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BARD1
NM_000465.4:c.1835A>T
NP_000456.2:p.(D612V)
Likely Benign
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BARD1
NM_000465.4:c.1868G>A
NP_000456.2:p.(G623E)
VUS
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BARD1
NM_000465.4:c.568G>A
NP_000456.2:p.(D190N)
VUS
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BARD1
NM_000465.4:c.562C>T
NP_000456.2:p.(P188S)
VUS
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BARD1
NM_000465.4:c.1409A>G
NP_000456.2:p.(N470S)
VUS
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BARD1
NM_000465.4:c.221G>T
NP_000456.2:p.(C74F)
VUS
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BARD1
NM_000465.4:c.1788del
NP_000456.2:p.(K596Nfs*9)
Pathogenic
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BARD1
NM_000465.4:c.1694G>A
NP_000456.2:p.(R565H)
Likely Benign
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BARD1
NM_000465.4:c.1325C>T
NP_000456.2:p.(P442L)
Likely Benign
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BARD1
NM_000465.4:c.1658C>G
NP_000456.2:p.(S553*)
Pathogenic
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BARD1
NM_000465.4:c.1217G>A
NP_000456.2:p.(R406Q)
VUS
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BARD1
NM_000465.4:c.928T>G
NP_000456.2:p.(S310A)
VUS
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BARD1
NM_000465.4:c.722C>G
NP_000456.2:p.(S241C)
Benign
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BARD1
NM_000465.4:c.764A>G
NP_000456.2:p.(N255S)
VUS
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BARD1
NM_000465.4:c.62G>T
NP_000456.2:p.(R21L)
VUS
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BARD1
NM_000465.4:c.2127A>G
NP_000456.2:p.(P709=)
VUS
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