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Gene MSH6
Variant S2*
Impact List nonsense
Protein Effect loss of function - predicted
Gene Variant Descriptions MSH6 S2* results in a premature truncation of the Msh6 protein at amino acid 2 of 1360 (UniProt.org). S2* has not been characterized, however, due to the loss of several functional domains including the ATPase domain (PMID: 17531815, PMID: 23391514), is predicted to lead to a loss of Msh6 protein function.
Associated Drug Resistance
Category Variants Paths

MSH6 mutant MSH6 inact mut MSH6 S2*

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Transcript NM_000179.3
gDNA chr2:g.47783238C>A
cDNA c.5C>A
Protein p.S2*
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406795.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001406800.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001281492.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001406809.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001406813.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001406802.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001406803.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_000179.3 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
XM_024452819.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001407362.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_000179.2 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001281492.2 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001406798.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001406817.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001406796.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38
NM_001406808.1 chr2:g.47783238C>A c.5C>A p.S2* RefSeq GRCh38/hg38

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