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Gene MSH6
Variant I872fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions MSH6 I872fs results in a change in the amino acid sequence of the Msh6 protein beginning at aa 872 of 1360, likely resulting in premature truncation of the functional protein (UniProt.org). I872fs (reported as I872fs*10) has not been biochemically characterized, but is associated with a loss of Msh6 protein expression and increased microsatellite instability in tumor samples (PMID: 14974087), 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 I872fs

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Transcript NM_000179.3
gDNA chr2:g.(47800596_47800597)
cDNA c.(2614_2613)
Protein p.I872fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406796.1 chr2:g.(47800596_47800597) c.(2614_2613) p.I872fs RefSeq GRCh38/hg38
NM_000179 chr2:g.(47800596_47800597) c.(2614_2613) p.I872fs RefSeq GRCh38/hg38
NM_001406798.1 chr2:g.(47800596_47800597) c.(2614_2613) p.I872fs RefSeq GRCh38/hg38
NM_001406800.1 chr2:g.(47800596_47800597) c.(2614_2613) p.I872fs RefSeq GRCh38/hg38
XM_024452819.1 chr2:g.(47800596_47800597) c.(2614_2613) p.I872fs RefSeq GRCh38/hg38
NM_001406809.1 chr2:g.(47800596_47800597) c.(2614_2613) p.I872fs RefSeq GRCh38/hg38
NM_000179.2 chr2:g.(47800596_47800597) c.(2614_2613) p.I872fs RefSeq GRCh38/hg38
NM_000179.3 chr2:g.(47800596_47800597) c.(2614_2613) p.I872fs RefSeq GRCh38/hg38
NM_001406808.1 chr2:g.(47800596_47800597) c.(2614_2613) p.I872fs RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
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  • 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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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

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