Gene Variant Detail

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Gene MLH1
Variant P403S
Impact List missense
Protein Effect no effect - predicted
Gene Variant Descriptions MLH1 P403S does not lie within any known functional domains of the Mlh1 protein (UniProt.org). P403S is predicted to be benign in in silico analyses (PMID: 22753075) and has mismatch repair activity similar to wild-type Mlh1 in an in vitro assay (PMID: 20020535), and therefore, is predicted to have no effect on Mlh1 protein function.
Associated Drug Resistance
Category Variants Paths

MLH1 mutant MLH1 P403S

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Transcript NM_000249.4
gDNA chr3:g.37025805C>T
cDNA c.1207C>T
Protein p.P403S
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000249 chr3:g.37025805C>T c.1207C>T p.P403S RefSeq GRCh38/hg38
NM_001258271 chr3:g.37025805C>T c.1207C>T p.P403S RefSeq GRCh38/hg38
NM_001258271.1 chr3:g.37025805C>T c.1207C>T p.P403S RefSeq GRCh38/hg38
NM_000249.4 chr3:g.37025805C>T c.1207C>T p.P403S RefSeq GRCh38/hg38
NM_001354628.1 chr3:g.37025805C>T c.1207C>T p.P403S RefSeq GRCh38/hg38
NM_001354630.1 chr3:g.37025805C>T c.1207C>T p.P403S RefSeq GRCh38/hg38
NM_001258271.2 chr3:g.37025805C>T c.1207C>T p.P403S RefSeq GRCh38/hg38
NM_001354630.2 chr3:g.37025805C>T c.1207C>T p.P403S RefSeq GRCh38/hg38
NM_000249.3 chr3:g.37025805C>T c.1207C>T p.P403S RefSeq GRCh38/hg38
NM_001354628.2 chr3:g.37025805C>T c.1207C>T p.P403S RefSeq GRCh38/hg38

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
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...
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 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 ovarian cancer not applicable N/A Guideline Risk Factor Germline mutations in MLH1 result in Lynch syndrome, which is associated with increased risk of ovarian 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...