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Gene MLH1
Variant H109P
Impact List missense
Protein Effect loss of function - predicted
Gene Variant Descriptions MLH1 H109P lies within the ATPase domain of the Mlh1 protein (PMID: 22753075). H109P results in a loss of mismatch repair activity of in an in vitro assay (PMID: 20020535), and therefore, is predicted to lead to a loss of Mlh1 protein function.
Associated Drug Resistance
Category Variants Paths

MLH1 mutant MLH1 inact mut MLH1 H109P

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Transcript NM_000249.4
gDNA chr3:g.37004420A>C
cDNA c.326A>C
Protein p.H109P
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_005265161.2 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
NM_000249.4 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
XM_005265161 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
NM_001354630.1 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
NM_000249 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
NM_000249.3 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
NM_001258271.1 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
NM_001354628.2 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
NM_001354628.1 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
NM_001258271 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
NM_001354630.2 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
NM_001258271.2 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38
XM_005265161.3 chr3:g.37004420A>C c.326A>C p.H109P RefSeq GRCh38/hg38

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References