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Gene | MLH1 |
Variant | R474W |
Impact List | missense |
Protein Effect | no effect - predicted |
Gene Variant Descriptions | MLH1 R474W lies within the EXO1-interacting region and bipartite NLS sequence of the Mlh1 protein (PMID: 22753075). R474W demonstrates no splicing defects (PMID: 18561205) and retains methylation sensitivity in culture (PMID: 30998989), and therefore, is predicted to have no effect on Mlh1 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
MLH1 mutant MLH1 R474W |
Transcript | NM_000249.4 |
gDNA | chr3:g.37028794C>T |
cDNA | c.1420C>T |
Protein | p.R474W |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000249.4 | chr3:g.37028794C>T | c.1420C>T | p.R474W | RefSeq | GRCh38/hg38 |
NM_001258271.2 | chr3:g.37028794C>T | c.1420C>T | p.R474W | RefSeq | GRCh38/hg38 |
NM_001354628.2 | chr3:g.37028794C>T | c.1420C>T | p.R474W | RefSeq | GRCh38/hg38 |
NM_001354630.2 | chr3:g.37028794C>T | c.1420C>T | p.R474W | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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