SNURF SNRPN upstream open reading frame

Information
Symbol
SNURF
Type
protein-coding
Description
SNRPN upstream open reading frame
Entrez Gene ID
8926
Genome
hg19
Position
chr15:25,200,134-25,213,968
Genome
hg38
Position
chr15:24,954,987-24,968,821
HGNC
HGNC:11171 HGNC
Ensembl
ENSG00000273173 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Conflicting classifications of pathogenicity 0 2
not provided 2 0
Uncertain significance 0 24
Ranking
ClinVar
0
0
2
22
0
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
HGNC HGNC:11171 HGNC
Ensembl ENSG00000273173 Ensembl
AllianceGenome HGNC:11171
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000577949.6 hg38 chr15 24,954,987 24,968,821 13,835
ENST00000338327.4 hg38 chr15 24,955,014 24,968,829 13,816
ENST00000577949.6 hg19 chr15 25,200,134 25,213,968 13,835
ENST00000338327.4 hg19 chr15 25,200,161 25,213,976 13,816
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