Project HERA
RNF43 variants
Every RNF43 variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
RNF43 variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
RNF43
NM_017763.6:c.662G>A
NP_060233.3:p.(R221Q)
VUS
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RNF43
NM_017763.5:c.1148T>C
NP_060233.3:p.(M383T)
Likely Benign
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RNF43
NM_017763.5:c.1403C>T
NP_060233.3:p.(S468L)
VUS
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RNF43
NM_017763.5:c.1196C>T
NP_060233.3:p.(P399L)
VUS
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RNF43
NM_017763.5:c.252+2C>G
NP_060233.3:p.?
Likely Pathogenic
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