MSH6 G1157S
Gene Variant Detail

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Gene MSH6
Variant G1157S
Impact List missense
Protein Effect loss of function - predicted
Gene Variant Descriptions MSH6 G1157S lies within the ATPase domain of the Msh6 protein (PMID: 17531815). G1157S results in splicing similar to wild-type Msh6 but decreased mismatch repair in an in vitro assay (PMID: 32849802), 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 G1157S

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Transcript NM_000179.3
gDNA chr2:g.47804940G>A
cDNA c.3469G>A
Protein p.G1157S
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406809.1 chr2:g.47804940G>A c.3469G>A p.G1157S RefSeq GRCh38/hg38
NM_001406800.1 chr2:g.47804940G>A c.3469G>A p.G1157S RefSeq GRCh38/hg38
XM_024452819.1 chr2:g.47804940G>A c.3469G>A p.G1157S RefSeq GRCh38/hg38
NM_001406808.1 chr2:g.47804940G>A c.3469G>A p.G1157S RefSeq GRCh38/hg38
NM_001406796.1 chr2:g.47804940G>A c.3469G>A p.G1157S RefSeq GRCh38/hg38
NM_000179.3 chr2:g.47804940G>A c.3469G>A p.G1157S RefSeq GRCh38/hg38
NM_000179.2 chr2:g.47804940G>A c.3469G>A p.G1157S RefSeq GRCh38/hg38
NM_001406795.1 chr2:g.47803620G>A c.3469G>A p.G1157S RefSeq GRCh38/hg38
NM_001406802.1 chr2:g.47803620G>A c.3469G>A p.G1157S RefSeq GRCh38/hg38

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