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Gene | MLH1 |
Variant | T117M |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | MLH1 T117M lies within the ATPase domain of the Mlh1 protein (PMID: 22753075). T117M confers a loss of function to the Mlh1 protein as demonstrated by reduced Pms2 and Mlh1 expression and loss of mismatch repair activity in culture (PMID: 36054288) and in in vitro assays (PMID: 20020535, PMID: 17510385) and has reduced protein expression as compared to wild-type Mlh1 (PMID: 17510385). |
Associated Drug Resistance | |
Category Variants Paths |
MLH1 mutant MLH1 inact mut MLH1 T117M |
Transcript | NM_000249.4 |
gDNA | chr3:g.37004444C>T |
cDNA | c.350C>T |
Protein | p.T117M |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001258271.1 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
NM_001354628.1 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
NM_001258271.2 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
NM_001354628.2 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
NM_001354630.1 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
XM_005265161.3 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
NM_001258271 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
NM_000249.4 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
NM_000249.3 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
NM_001354630.2 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
XM_005265161 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
NM_000249 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
XM_005265161.2 | chr3:g.37004444C>T | c.350C>T | p.T117M | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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