Project HERA
AXIN2 variants
Every AXIN2 variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
AXIN2 variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
AXIN2
NM_004655.4:c.2433G>A
NP_004646.3:p.(E811=)
VUS
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AXIN2
NM_004655.4:c.203G>A
NP_004646.3:p.(R68Q)
VUS
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AXIN2
NM_004655.4:c.1059+8C>T
NP_004646.3:p.?
VUS
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AXIN2
NM_004655.4:c.2051C>T
NP_004646.3:p.(A684V)
VUS
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AXIN2
NM_004655.4:c.1365A>T
NP_004646.3:p.(P455=)
VUS
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AXIN2
NM_004655.4:c.1530G>A
NP_004646.3:p.(T510=)
Likely Benign
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AXIN2
NM_004655.4:c.1235A>G
NP_004646.3:p.(N412S)
Likely Benign
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AXIN2
NM_004655.4:c.1713-18G>A
NP_004646.3:p.?
VUS
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AXIN2
NM_004655.4:c.1985T>C
NP_004646.3:p.(L662P)
VUS
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AXIN2
NM_004655.4:c.1168A>G
NP_004646.3:p.(S390G)
Likely Benign
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AXIN2
NM_004655.4:c.405C>T
NP_004646.3:p.(Y135=)
VUS
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AXIN2
NM_004655.4:c.2013_2024del
NP_004646.3:p.(T672_R675del)
Benign
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AXIN2
NM_004655.4:c.1908-23C>T
NP_004646.3:p.?
VUS
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AXIN2
NM_004655.4:c.432T>C
NP_004646.3:p.(I144=)
Benign
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