MSH5-SAPCD1 MSH5-SAPCD1 readthrough (NMD candidate)

Information
Symbol
MSH5-SAPCD1
Type
ncRNA
Description
MSH5-SAPCD1 readthrough (NMD candidate)
Entrez Gene ID
100532732
Genome
hg19
Position
chr6:31,707,797-31,732,627
Genome
hg38
Position
chr6:31,740,020-31,764,850
HGNC
HGNC:41994 HGNC
Ensembl
ENSG00000255152 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 6
Benign 0 18
Likely benign 0 28
not provided 10 0
Uncertain significance 0 82
Ranking
ClinVar
0
0
8
124
6
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 MSH5-C6orf26
HGNC HGNC:41994 HGNC
Ensembl ENSG00000255152 Ensembl
AllianceGenome HGNC:41994
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000493662.6 hg38 chr6 31,740,020 31,764,850 24,831
ENST00000493662.6 hg19 chr6 31,707,797 31,732,627 24,831
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