Project HERA
MET variants
Every MET variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
MET variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
MET
NM_001127500.2:c.3082G>C
NP_001120972.1:p.(D1028H)
VUS
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MET
NM_001127500.3:c.1063G>A
NP_001120972.1:p.(E355K)
VUS
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MET
NM_001127500.2:c.737C>T
NP_001120972.1:p.(P246L)
VUS
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MET
NM_001127500.3:c.226G>A
NP_001120972.1:p.(E76K)
VUS
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MET
NM_001127500.3:c.156_157delinsTT
NP_001120972.1:p.(Q53*)
Likely Pathogenic
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MET
NM_001127500.3:c.3852+5T>C
NP_001120972.1:p.?
Likely Benign
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MET
NM_001127500.3:c.110T>C
NP_001120972.1:p.(V37A)
Likely Benign
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