TNFSF12-TNFSF13 TNFSF12-TNFSF13 readthrough

Information
Symbol
TNFSF12-TNFSF13
Type
protein-coding
Description
TNFSF12-TNFSF13 readthrough
Entrez Gene ID
407977
Genome
hg19
Position
chr17:7,452,416-7,464,918
Genome
hg38
Position
chr17:7,549,099-7,561,601
HGNC
HGNC:33537 HGNC
Ensembl
ENSG00000248871 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 36
Likely benign 0 176
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 240
Ranking
ClinVar
0
0
40
408
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
SYNONYM TWE-PRIL
HGNC HGNC:33537 HGNC
Ensembl ENSG00000248871 Ensembl
AllianceGenome HGNC:33537
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000293826.4 hg38 chr17 7,549,099 7,561,601 12,503
ENST00000293826.4 hg19 chr17 7,452,416 7,464,918 12,503
Genome browser