MSH4 mutS homolog 4

Information
Symbol
MSH4
Type
protein-coding
Description
mutS homolog 4
Entrez Gene ID
4438
Genome
hg19
Position
chr1:76,262,567-76,378,927
Genome
hg38
Position
chr1:75,796,882-75,913,242
MIM
602105 OMIM
HGNC
HGNC:7327 HGNC
Ensembl
ENSG00000057468 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 16
Likely pathogenic 0 16
Benign 0 14
Likely benign 0 4
Uncertain significance 0 94
Ranking
ClinVar
0
0
2
116
24
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM ASG
SYNONYM POF20
SYNONYM SPGF2
MIM 602105 OMIM
HGNC HGNC:7327 HGNC
Ensembl ENSG00000057468 Ensembl
AllianceGenome HGNC:7327
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000263187.4 hg38 chr1 75,796,882 75,913,242 116,361
ENST00000263187.4 hg19 chr1 76,262,567 76,378,927 116,361
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