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Gene MLH1
Variant R217C
Impact List missense
Protein Effect unknown
Gene Variant Descriptions MLH1 R217C lies within the ATPase domain of the Mlh1 protein (PMID: 22753075). The functional effect of R217C is conflicting, as it demonstrates mismatch repair activity similar to wild-type Mlh1 in a cell based assay (PMID: 11781295), but also results in impaired interaction with Pms2 (PMID: 27173243), and therefore, its effect on Mlh1 protein function is unknown.
Associated Drug Resistance
Category Variants Paths

MLH1 mutant MLH1 R217C

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Transcript NM_000249.4
gDNA chr3:g.37012071C>T
cDNA c.649C>T
Protein p.R217C
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001354624.2 chr3:g.37042323_37042325delAGGinsTGT c.649_651delAGGinsTGT p.R217C RefSeq GRCh38/hg38
NM_001258271.1 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
NM_001354628.1 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
NM_000249.4 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
NM_000249 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
NM_000249.3 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
NM_001354625.1 chr3:g.37042323_37042325delAGGinsTGT c.649_651delAGGinsTGT p.R217C RefSeq GRCh38/hg38
NM_001354627.2 chr3:g.37042323_37042325delAGGinsTGT c.649_651delAGGinsTGT p.R217C RefSeq GRCh38/hg38
XM_005265161 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
XM_017006451 chr3:g.37042323_37042325delAGGinsTGT c.649_651delAGGinsTGT p.R217C RefSeq GRCh38/hg38
NM_001354626.1 chr3:g.37042323_37042325delAGGinsTGT c.649_651delAGGinsTGT p.R217C RefSeq GRCh38/hg38
NM_001354630.1 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
NM_001258271.2 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
NM_001354627.1 chr3:g.37042323_37042325delAGGinsTGT c.649_651delAGGinsTGT p.R217C RefSeq GRCh38/hg38
NM_001354630.2 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
NM_001354628.2 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
NM_001354624.1 chr3:g.37042323_37042325delAGGinsTGT c.649_651delAGGinsTGT p.R217C RefSeq GRCh38/hg38
NM_001354626.2 chr3:g.37042323_37042325delAGGinsTGT c.649_651delAGGinsTGT p.R217C RefSeq GRCh38/hg38
NM_001258271 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
XM_011533727 chr3:g.37042323_37042325delAGGinsTGT c.649_651delAGGinsTGT p.R217C RefSeq GRCh38/hg38
XM_005265161.2 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38
NM_001354625.2 chr3:g.37042323_37042325delAGGinsTGT c.649_651delAGGinsTGT p.R217C RefSeq GRCh38/hg38
XM_005265161.3 chr3:g.37012071C>T c.649C>T p.R217C RefSeq GRCh38/hg38

Filtering

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  • 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

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.

Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References