Graphs & statistics on gene MSH2

Variant type (DNA level, all public variants)
All public variants (4)
Substitutions
Substitutions
100%

 
Unique public variants (4)
Substitutions
Substitutions
100%

 
Variant type (DNA level, all public pathogenic variants)
All public pathogenic variants (3)
Substitutions
Substitutions
100%

 
Unique public pathogenic variants (3)
Substitutions
Substitutions
100%

 
Variant type (Protein level, all public variants) (note: numbers are sums for all transcripts of this gene)
All public variants (4)
Unknown
Missense changes
Silent changes
Stop changes
Unknown
25%
Missense changes
25%
Silent changes
25%
Stop changes
25%

 
Unique public variants (4)
Unknown
Missense changes
Silent changes
Stop changes
Unknown
25%
Missense changes
25%
Silent changes
25%
Stop changes
25%

 
Variant type (Protein level, all public pathogenic variants) (note: numbers are sums for all transcripts of this gene)
All public pathogenic variants (3)
Unknown
Missense changes
Stop changes
Unknown
33%
Missense changes
33%
Stop changes
33%

 
Unique public pathogenic variants (3)
Unknown
Missense changes
Stop changes
Unknown
33%
Missense changes
33%
Stop changes
33%

 
Variant location (DNA level, all public variants) (note: numbers are sums for all transcripts of this gene)
All public variants (4)
Coding
Splice region
Coding
75%
Splice region
25%

 
Unique public variants (4)
Coding
Splice region
Coding
75%
Splice region
25%

 
Variant type (DNA level, all public pathogenic variants) (note: numbers are sums for all transcripts of this gene)
All public pathogenic variants (3)
Coding
Splice region
Coding
67%
Splice region
33%

 
Unique public pathogenic variants (3)
Coding
Splice region
Coding
67%
Splice region
33%