Gene Variant Detail

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Gene MLH1
Variant T81I
Impact List missense
Protein Effect unknown
Gene Variant Descriptions MLH1 T81I lies within the ATPase domain of the Mlh1 protein (PMID: 22753075). T81I has not been characterized in the scientific literature and therefore, its effect on Mlh1 protein function is unknown (PubMed, Apr 2022).
Associated Drug Resistance

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Transcript NM_000249.3
gDNA chr3:g.37000989C>T
cDNA c.242C>T
Protein p.T81I
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001258271 chr3:g.37000989C>T c.242C>T p.T81I RefSeq GRCh38/hg38
XM_005265161.2 chr3:g.37000989C>T c.242C>T p.T81I RefSeq GRCh38/hg38
NM_001258271.1 chr3:g.37000989C>T c.242C>T p.T81I RefSeq GRCh38/hg38
NM_000249.3 chr3:g.37000989C>T c.242C>T p.T81I RefSeq GRCh38/hg38
NM_001354629.1 chr3:g.37004435C>T c.242C>T p.T81I RefSeq GRCh38/hg38
NM_001354630.1 chr3:g.37000989C>T c.242C>T p.T81I RefSeq GRCh38/hg38
NM_000249 chr3:g.37000989C>T c.242C>T p.T81I RefSeq GRCh38/hg38
XM_005265161 chr3:g.37000989C>T c.242C>T p.T81I RefSeq GRCh38/hg38
NM_001354628.1 chr3:g.37000989C>T c.242C>T p.T81I RefSeq GRCh38/hg38

Filtering

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  • Simple literal full or partial string matches
  • Separate multiple filter terms with a spaces, order doesn't matter (a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page, filtering has no impact on query parameters
  • Use quotes to match a longer phrase which contains spaces "mtor c1483f"

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
MLH1 mutant rectum cancer not applicable N/A Guideline Risk Factor Lynch syndrome results from germline mutations in DNA mismatch repair genes including MLH1, MSH2, MSH6, and PMS2, and is associated with increased risk of developing colorectal cancer (NCCN.org). detail...
MLH1 mutant small intestine adenocarcinoma not applicable N/A Guideline Risk Factor Lynch syndrome results from germline mutations in DNA mismatch repair genes including MLH1, MSH2, MSH6, and PMS2, and is associated with increased risk of developing small bowel adenocarcinoma (NCCN.org). detail...
MLH1 mutant colon cancer not applicable N/A Guideline Risk Factor Lynch syndrome results from germline mutations in DNA mismatch repair genes including MLH1, MSH2, MSH6, and PMS2, and is associated with increased risk of developing colon cancer (NCCN.org). detail...
MLH1 mutant pancreatic cancer not applicable N/A Guideline Risk Factor Germline mutations in MLH1 result in Lynch syndrome, which is associated with increased risk of developing pancreatic cancer (NCCN.org). detail...
MLH1 mutant endometrial carcinoma not applicable N/A Guideline Risk Factor Germline mutations in MLH1 result in Lynch syndrome, which is associated with increased risk of developing endometrial carcinoma (NCCN.org). detail...
MLH1 mutant stomach cancer not applicable N/A Guideline Risk Factor Germline mutations in MLH1 result in Lynch syndrome, which is associated with increased risk of early onset of gastric cancer (NCCN.org). detail...
Molecular Profile Protein Effect Treatment Approaches
MLH1 T81I unknown