Gene Variant Detail

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Gene MLH1
Variant S368L
Impact List missense
Protein Effect unknown
Gene Variant Descriptions MLH1 S368L does not lie within any known functional domains of the Mlh1 protein (UniProt.org). S368L 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.37025701C>T
cDNA c.1103C>T
Protein p.S368L
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001258271.1 chr3:g.37025701C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
NM_000249 chr3:g.37025701C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
NM_001354630.1 chr3:g.37025701C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
XM_017006451 chr3:g.37050559C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
NM_001354625.1 chr3:g.37050559C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
NM_001354627.1 chr3:g.37050559C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
NM_001354629.1 chr3:g.37025799_37025800delAGinsCT c.1102_1103delAGinsCT p.S368L RefSeq GRCh38/hg38
NM_001354626.1 chr3:g.37050559C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
NM_001258271 chr3:g.37025701C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
NM_001167617.2 chr3:g.37025994_37025995delTCinsCT c.1102_1103delTCinsCT p.S368L RefSeq GRCh38/hg38
NM_000249.3 chr3:g.37025701C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
NM_001354624.1 chr3:g.37050559C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
XM_011533727 chr3:g.37050559C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
NM_001354628.1 chr3:g.37025701C>T c.1103C>T p.S368L RefSeq GRCh38/hg38
NM_001354620.1 chr3:g.37025994_37025995delTCinsCT c.1102_1103delTCinsCT p.S368L RefSeq GRCh38/hg38
NM_001167617 chr3:g.37025994_37025995delTCinsCT c.1102_1103delTCinsCT p.S368L RefSeq GRCh38/hg38

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  • 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 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 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 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 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...
Molecular Profile Protein Effect Treatment Approaches
MLH1 S368L unknown