Gene Variant Detail

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Gene MLH1
Variant A21V
Impact List missense
Protein Effect loss of function - predicted
Gene Variant Descriptions MLH1 A21V lies within the ATPase domain of the Mlh1 protein (PMID: 22753075). A21V results in defective mismatch repair (MMR) activity in a functional screen in cultured mouse cells (PMID: 31784484), and therefore, is predicted to lead to a loss of Mlh1 protein function.
Associated Drug Resistance
Category Variants Paths

MLH1 mutant MLH1 inact mut MLH1 A21V

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Transcript NM_000249.4
gDNA chr3:g.36993609C>T
cDNA c.62C>T
Protein p.A21V
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000249.4 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
NM_001354628.2 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
NM_001354629.1 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
NM_000249.3 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
XM_005265161.2 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
NM_001258271.1 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
NM_001354629.2 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
NM_001354628.1 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
XM_005265161.3 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
NM_001354630.1 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
NM_001258271.2 chr3:g.36993609C>T c.62C>T p.A21V RefSeq GRCh38/hg38
NM_001354630.2 chr3:g.36993609C>T c.62C>T p.A21V 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 )
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Sorting

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Molecular Profile Protein Effect Treatment Approaches
MLH1 A21V loss of function - predicted