Project HERA
MSH3 variants
Every MSH3 variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
MSH3 variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
MSH3
NM_002439.5:c.1897-12T>A
NP_002430.3:p.?
VUS
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MSH3
NM_002439.5:c.2006G>A
NP_002430.3:p.(R669Q)
VUS
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MSH3
NM_002439.5:c.131C>G
NP_002430.3:p.(A44G)
VUS
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MSH3
NM_002439.5:c.495A>G
NP_002430.3:p.(K165=)
VUS
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MSH3
NM_002439.5:c.1567G>A
NP_002430.3:p.(E523K)
Likely Benign
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MSH3
NM_002439.5:c.1522A>G
NP_002430.3:p.(K508E)
Likely Benign
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MSH3
NM_002439.5:c.1360C>T
NP_002430.3:p.(R454*)
Likely Pathogenic
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MSH3
NM_002439.5:c.316C>G
NP_002430.3:p.(Q106E)
VUS
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MSH3
NM_002439.5:c.316C>G
NP_002430.3:p.(Q106E)
VUS
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MSH3
NM_002439.5:c.2041C>T
NP_002430.3:p.(P681S)
VUS
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MSH3
NM_002439.5:c.2800G>T
NP_002430.3:p.(G934C)
VUS
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MSH3
NM_002439.5:c.8G>A
NP_002430.3:p.(R3H)
Likely Benign
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MSH3
NM_002439.5:c.2436-13G>T
NP_002430.3:p.?
VUS
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