Project HERA
IDH2 variants
Every IDH2 variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
IDH2 variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
IDH2
NM_002168.2:c.374-10G>A
NP_002159.2:p.?
VUS
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IDH2
NM_002168.3:c.413C>A
NP_002159.2:p.(T138N)
VUS
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IDH2
NM_002168.3:c.413C>A
NP_002159.2:p.(T138N)
VUS
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IDH2
NM_002168.3:c.413C>A
NP_002159.2:p.(T138N)
VUS
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IDH2
NM_002168.3:c.520G>A
NP_002159.2:p.(A174T)
VUS
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IDH2
NM_002168.3:c.413C>A
NP_002159.2:p.(T138N)
VUS
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IDH2
NM_002168.3:c.413C>A
NP_002159.2:p.(T138N)
VUS
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IDH2
NM_002168.3:c.413C>A
NP_002159.2:p.(T138N)
VUS
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IDH2
NM_002168.3:c.413C>A
NP_002159.2:p.(T138N)
VUS
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IDH2
NM_002168.3:c.514A>G
NP_002159.2:p.(R172G)
Pathogenic
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IDH2
NM_002168.3:c.419G>A
NP_002159.2:p.(R140Q)
Pathogenic
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IDH2
NM_002168.3:c.516G>C
NP_002159.2:p.(R172S)
VUS
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IDH2
NM_002168.3:c.515G>A
NP_002159.2:p.(R172K)
VUS
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IDH2
NM_002168.3:c.515G>T
NP_002159.2:p.(R172M)
Likely Pathogenic
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IDH2
NM_002168.2:c.430G>C
NP_002159.2:p.(G144R)
VUS
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