MSH6 S360I
Gene Variant Detail

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Gene MSH6
Variant S360I
Impact List missense
Protein Effect unknown
Gene Variant Descriptions MSH6 S360I lies within an MSH2-binding region of the Msh6 protein (PMID: 12019211). S360I is predicted to have no effect on Msh6 protein function by computational analysis (PMID: 23621914), but has not been biochemically characterized and therefore, its effect on Msh6 protein function is unknown (PubMed, Oct 2025).
Associated Drug Resistance
Category Variants Paths

MSH6 mutant MSH6 S360I

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Transcript NM_000179.3
gDNA chr2:g.47799062G>T
cDNA c.1079G>T
Protein p.S360I
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406803.1 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_001406827.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_000179.3 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_001406808.1 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_001406805.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406820.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406800.1 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_001406797.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406795.1 chr2:g.47798966G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_001406822.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_000179.2 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_001406821.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406818.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406830.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
XM_024452819.1 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_001406819.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
XM_011532799 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406825.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406802.1 chr2:g.47798966G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_000179 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_001406817.1 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
XM_024452821.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406809.1 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_001406798.1 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38
NM_001406801.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406824.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406828.1 chr2:g.47799358_47799359delTCinsAT c.1078_1079delTCinsAT p.S360I RefSeq GRCh38/hg38
NM_001406796.1 chr2:g.47799062G>T c.1079G>T p.S360I RefSeq GRCh38/hg38

Filtering

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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.
  • Click on any column header arrows to sort by that column
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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References