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| Gene | MLH1 |
| Variant | Q60P |
| Impact List | missense |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | MLH1 Q60P lies within the ATPase domain of the Mlh1 protein (PMID: 22753075). Q60P results in partial loss of DNA mismatch repair activity in a yeast assay (PMID: 15475387), 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 Q60P |
| Transcript | NM_000249.4 |
| gDNA | chr3:g.36996681A>C |
| cDNA | c.179A>C |
| Protein | p.Q60P |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_005265161.3 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| XM_005265163 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354630.1 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| XM_047448153.1 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354618.2 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354617.2 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001258274.3 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354619.1 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354616.1 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354615.1 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001167619.3 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354628.1 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_000249 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| XM_005265164 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354628.2 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001167618.3 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001258274 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001258271.1 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354629.1 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354617.1 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001258273.1 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001167619.2 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| XM_047448154.1 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354619.2 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354630.2 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354615.2 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001258273 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001167619 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001167618 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| XM_005265161.2 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001167618.2 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_000249.4 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354629.2 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_000249.3 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001258274.2 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| XM_047448155.1 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001258271 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| XM_005265161 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001258271.2 | chr3:g.36996681A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354618.1 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001354616.2 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| NM_001258273.2 | chr3:g.37020327A>C | c.179A>C | p.Q60P | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|