Project HERA
KRAS variants
Every KRAS variant the pipeline has interpreted, classified against the ClinGen expert-panel specification for the gene where one exists.
KRAS variants
Newest first. Each row opens the full report, criterion by criterion.
Variant
Protein change
Classification
KRAS
NM_033360.4:c.292G>T
NP_203524.1:p.(E98*)
VUS
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KRAS
NM_033360.3:c.35G>T
NP_203524.1:p.(G12V)
VUS
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KRAS
NM_033360.2:c.57G>T
NP_203524.1:p.(L19F)
VUS
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KRAS
NM_033360.3:c.250A>G
NP_203524.1:p.(I84V)
VUS
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KRAS
NM_033360.4:c.407G>A
NP_203524.1:p.(S136N)
—
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KRAS
NM_033360.4:c.40G>A
NP_203524.1:p.(V14I)
Pathogenic
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KRAS
NM_033360.4:c.183A>C
NP_203524.1:p.(Q61H)
Likely Pathogenic
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KRAS
NM_033360.3:c.35_37delinsATT
NP_203524.1:p.(G12_G13delinsDC)
VUS
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KRAS
NM_033360.4:c.-11-30T>C
NP_203524.1:p.?
Likely Benign
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KRAS
NM_033360.3:c.460G>A
NP_203524.1:p.(D154N)
VUS
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KRAS
NM_033360.3:c.34_35delinsTGTGC
NP_203524.1:p.(G12delinsCA)
VUS
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KRAS
NM_033360.3:c.179G>T
NP_203524.1:p.(G60V)
Likely Pathogenic
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KRAS
NM_004985.4:c.178G>C
NP_004976.2:p.(G60R)
Likely Pathogenic
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KRAS
NM_001369787.1:c.531_533del
NP_001356716.1:p.(K180del)
Benign
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KRAS
NM_001369787.1:c.508A>T
NP_001356716.1:p.(M170L)
VUS
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KRAS
NM_004985.4:c.24A>G
NP_004976.2:p.(V8=)
Benign
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KRAS
NM_001369786.1:c.194G>T
NP_001356715.1:p.(S65I)
VUS
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KRAS
NM_004985.4:c.173C>T
NP_004976.2:p.(T58I)
VUS
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KRAS
NM_001369786.1:c.101C>T
NP_001356715.1:p.(P34L)
Likely Pathogenic
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KRAS
NM_001369786.1:c.15A>T
NP_001356715.1:p.(K5N)
VUS
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KRAS
NM_001369786.1:c.40G>A
NP_001356715.1:p.(V14I)
VUS
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KRAS
NM_001369787.1:c.519T>C
NP_001356716.1:p.(D173=)
Benign
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KRAS
NM_001369786.1:c.65A>G
NP_001356715.1:p.(Q22R)
VUS
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KRAS
NM_001369787.1:c.451-14T>C
NP_001356716.1:p.?
VUS
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KRAS
NM_033360.2:c.34G>C
NP_203524.1:p.(G12R)
Likely Pathogenic
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