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Gene MSH6
Variant K1013N
Impact List missense
Protein Effect unknown
Gene Variant Descriptions MSH6 K1013N lies within the lever domain of the Msh2 protein (PMID: 17531815). K1013N has not been characterized in the scientific literature and therefore, its effect on Msh6 protein function is unknown (PubMed, Oct 2023).
Associated Drug Resistance
Category Variants Paths

MSH6 mutant MSH6 K1013N

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Transcript NM_000179.3
gDNA chr2:g.47801022G>C
cDNA c.3039G>C
Protein p.K1013N
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001281493.2 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001281494 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406809.1 chr2:g.47801022G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406814.1 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001281494.2 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406816.1 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001281494.1 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001281493 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406811.1 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_000179.2 chr2:g.47801022G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_000179.3 chr2:g.47801022G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406808.1 chr2:g.47801022G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406815.1 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406796.1 chr2:g.47801022G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
XM_024452819.1 chr2:g.47801022G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406823.1 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406812.1 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406829.1 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406798.1 chr2:g.47801022G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_000179 chr2:g.47801022G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001281493.1 chr2:g.47806595G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38
NM_001406800.1 chr2:g.47801022G>C c.3039G>C p.K1013N RefSeq GRCh38/hg38

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