Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | MLH1 |
Variant | E663A |
Impact List | missense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | MLH1 E663A lies within the EXO1-interacting region and the C-terminal dimerization domain of the Mlh1 protein (PMID: 22753075). E663A results in decreased mismatch repair (MMR) activity in a functional screen in cultured mouse cells (PMID: 31784484), 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 E663A |
Transcript | NM_000249.4 |
gDNA | chr3:g.37048608A>C |
cDNA | c.1988A>C |
Protein | p.E663A |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000249.3 | chr3:g.37048608A>C | c.1988A>C | p.E663A | RefSeq | GRCh38/hg38 |
NM_001354628.2 | chr3:g.37048995A>C | c.1988A>C | p.E663A | RefSeq | GRCh38/hg38 |
NM_001354628.1 | chr3:g.37048995A>C | c.1988A>C | p.E663A | RefSeq | GRCh38/hg38 |
NM_000249.4 | chr3:g.37048608A>C | c.1988A>C | p.E663A | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|