SNRPF-DT SNRPF divergent transcript

Information
Symbol
SNRPF-DT
Type
ncRNA
Description
SNRPF divergent transcript
Entrez Gene ID
105369921
Genome
hg19
Position
chr12:96,185,511-96,252,604
Genome
hg38
Position
chr12:95,791,733-95,858,826
HGNC
HGNC:55452 HGNC
Ensembl
ENSG00000258343 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
[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
HGNC HGNC:55452 HGNC
Ensembl ENSG00000258343 Ensembl
AllianceGenome HGNC:55452
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000553194.1 hg38 chr12 95,795,345 95,858,839 63,495
ENST00000670743.1 hg38 chr12 95,791,733 95,858,826 67,094
ENST00000670743.1 hg19 chr12 96,185,511 96,252,604 67,094
ENST00000553194.1 hg19 chr12 96,189,123 96,252,617 63,495
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