TNFRSF13C TNF receptor superfamily member 13C

Information
Symbol
TNFRSF13C
Type
protein-coding
Description
TNF receptor superfamily member 13C
Entrez Gene ID
115650
Genome
hg19
Position
chr22:42,318,036-42,322,810
Genome
hg38
Position
chr22:41,922,032-41,926,806
MIM
606269 OMIM
HGNC
HGNC:17755 HGNC
Ensembl
ENSG00000159958 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 2
Benign 0 22
Likely benign 0 104
Conflicting classifications of pathogenicity 0 26
Uncertain significance 0 164
Ranking
ClinVar
0
0
18
268
2
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 BAFF-R
SYNONYM BAFFR
SYNONYM BROMIX
SYNONYM CD268
SYNONYM CVID4
SYNONYM prolixin
MIM 606269 OMIM
HGNC HGNC:17755 HGNC
Ensembl ENSG00000159958 Ensembl
AllianceGenome HGNC:17755
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000291232.5 hg38 chr22 41,922,032 41,926,806 4,775
ENST00000291232.5 hg19 chr22 42,318,036 42,322,810 4,775
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