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Gene MSH6
Variant P768H
Impact List missense
Protein Effect unknown
Gene Variant Descriptions MSH6 P768H lies within the lever domain of the Msh6 protein (PMID: 17531815). P768H has not been characterized in the scientific literature and therefore, its effect on Msh6 protein function is unknown (PubMed, Jun 2024).
Associated Drug Resistance
Category Variants Paths

MSH6 mutant MSH6 P768H

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Transcript NM_000179.3
gDNA chr2:g.47800286C>A
cDNA c.2303C>A
Protein p.P768H
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001281492 chr2:g.47800676C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_001406798.1 chr2:g.47800286C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_001406800.1 chr2:g.47800286C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
XM_024452819.1 chr2:g.47800286C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_000179.2 chr2:g.47800286C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_001406803.1 chr2:g.47800286C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_001406796.1 chr2:g.47800286C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_000179.3 chr2:g.47800286C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_001406809.1 chr2:g.47800286C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_000179 chr2:g.47800286C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_001406808.1 chr2:g.47800286C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_001281492.2 chr2:g.47800676C>A c.2303C>A p.P768H RefSeq GRCh38/hg38
NM_001281492.1 chr2:g.47800676C>A c.2303C>A p.P768H RefSeq GRCh38/hg38

Filtering

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Sorting

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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries