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Gene MLH1
Variant H329P
Impact List missense
Protein Effect unknown
Gene Variant Descriptions MLH1 H329P lies within the ATPase domain of the Mlh1 protein (PMID: 22753075). H329P results in altered subcellular localization and reduced protein expression (PMID: 21120944), decreased mismatch repair (MMR) activity in yeast (PMID: 17510385), but demonstrates proficient mismatch repair activity (PMID: 21120944), and ATPase activity, suppression of interstitial telomeric sequences, and localization to double-strand break sites (DSBs) similar to wild-type Mlh1 in cultured cells (PMID: 29544212), and therefore, its effect on Mlh1 protein function is unknown.
Associated Drug Resistance
Category Variants Paths

MLH1 mutant MLH1 H329P

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Transcript NM_000249.4
gDNA chr3:g.37020411A>C
cDNA c.986A>C
Protein p.H329P
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000249 chr3:g.37020411A>C c.986A>C p.H329P RefSeq GRCh38/hg38
NM_001354628.1 chr3:g.37020411A>C c.986A>C p.H329P RefSeq GRCh38/hg38
NM_001354630.1 chr3:g.37020411A>C c.986A>C p.H329P RefSeq GRCh38/hg38
NM_000249.4 chr3:g.37020411A>C c.986A>C p.H329P RefSeq GRCh38/hg38
NM_001258271.2 chr3:g.37020411A>C c.986A>C p.H329P RefSeq GRCh38/hg38
NM_000249.3 chr3:g.37020411A>C c.986A>C p.H329P RefSeq GRCh38/hg38
NM_001354630.2 chr3:g.37020411A>C c.986A>C p.H329P RefSeq GRCh38/hg38
NM_001258271 chr3:g.37020411A>C c.986A>C p.H329P RefSeq GRCh38/hg38
NM_001354628.2 chr3:g.37020411A>C c.986A>C p.H329P RefSeq GRCh38/hg38
NM_001258271.1 chr3:g.37020411A>C c.986A>C p.H329P RefSeq GRCh38/hg38

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  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

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