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Gene | MSH6 |
Variant | L821P |
Impact List | missense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | MSH6 L821P lies within the lever domain of the Msh6 protein (PMID: 17531815). L821P (corresponds to L818P in mouse) results in impaired mismatch binding and deficient mismatch repair activity in in vitro assays (PMID: 31965077), and therefore, is predicted to lead to a loss of Msh6 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
MSH6 mutant MSH6 inact mut MSH6 L821P |
Transcript | NM_000179.3 |
gDNA | chr2:g.47800445T>C |
cDNA | c.2462T>C |
Protein | p.L821P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000179.3 | chr2:g.47800445T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_001406800.1 | chr2:g.47800445T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_001406796.1 | chr2:g.47800445T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_001406798.1 | chr2:g.47800445T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_001406809.1 | chr2:g.47800445T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_001406799.1 | chr2:g.47800969_47800970delTTinsCC | c.2461_2462delTTinsCC | p.L821P | RefSeq | GRCh38/hg38 |
XM_024452819.1 | chr2:g.47800445T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_001406807.1 | chr2:g.47800969_47800970delTTinsCC | c.2461_2462delTTinsCC | p.L821P | RefSeq | GRCh38/hg38 |
NM_001406808.1 | chr2:g.47800445T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_000179.2 | chr2:g.47800445T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_000179 | chr2:g.47800445T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_001281492 | chr2:g.47800835T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_001406806.1 | chr2:g.47800969_47800970delTTinsCC | c.2461_2462delTTinsCC | p.L821P | RefSeq | GRCh38/hg38 |
NM_001281492.2 | chr2:g.47800835T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
NM_001281492.1 | chr2:g.47800835T>C | c.2462T>C | p.L821P | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
MSH6 L821P | loss of function - predicted |