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Gene MSH6
Variant R1095H
Impact List missense
Protein Effect no effect
Gene Variant Descriptions MSH6 R1095H lies within the ATPase domain of the Msh6 protein (PMID: 17531815). R1095H demonstrates DNA mismatch repair activity, expression, and MSH2-interaction ability similar to wild-type Msh6 protein in cell culture (PMID: 24040339, PMID: 21120944, PMID: 12522549).
Associated Drug Resistance
Category Variants Paths

MSH6 mutant MSH6 R1095H

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Transcript NM_000179.3
gDNA chr2:g.47803531G>A
cDNA c.3284G>A
Protein p.R1095H
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000179 chr2:g.47803531G>A c.3284G>A p.R1095H RefSeq GRCh38/hg38
NM_000179.3 chr2:g.47803531G>A c.3284G>A p.R1095H RefSeq GRCh38/hg38
NM_000179.2 chr2:g.47803531G>A c.3284G>A p.R1095H RefSeq GRCh38/hg38
NM_001406796.1 chr2:g.47803531G>A c.3284G>A p.R1095H RefSeq GRCh38/hg38
NM_001406808.1 chr2:g.47803531G>A c.3284G>A p.R1095H RefSeq GRCh38/hg38
XM_024452819.1 chr2:g.47803531G>A c.3284G>A p.R1095H RefSeq GRCh38/hg38
NM_001406809.1 chr2:g.47803531G>A c.3284G>A p.R1095H RefSeq GRCh38/hg38
NM_001406800.1 chr2:g.47803531G>A c.3284G>A p.R1095H RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. 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 on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
MSH6 mutant ovarian cancer not applicable N/A Guideline Risk Factor Germline mutations in MSH6 result in Lynch syndrome, which is associated with increased risk of ovarian cancer (NCCN.org). detail...
MSH6 mutant pancreatic cancer not applicable N/A Guideline Risk Factor Germline mutations in MSH6 result in Lynch syndrome, which is associated with increased risk of developing pancreatic cancer (NCCN.org). detail...
MSH6 mutant endometrial carcinoma not applicable N/A Guideline Risk Factor Germline mutations in MSH6 result in Lynch syndrome, which is associated with increased risk of developing endometrial carcinoma (NCCN.org). detail...
MSH6 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...
MSH6 mutant colorectal cancer not applicable N/A Clinical Study Diagnostic Germline mutations in MSH6 are associated with microsatellite instability in colorectal cancer (CRC), and are diagnostic for Lynch syndrome (hereditary nonpolyposis colorectal cancer) in colorectal cancer patients (PMID: 26582061; PMID: 19125127). 26582061 19125127
MSH6 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...
MSH6 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...
MSH6 mutant stomach cancer not applicable N/A Guideline Risk Factor Germline mutations in MSH6 result in Lynch syndrome, which is associated with increased risk of developing pancreatic cancer (NCCN.org). detail...