RELT RELT TNF receptor

Information
Symbol
RELT
Type
protein-coding
Description
RELT TNF receptor
Entrez Gene ID
84957
Genome
hg19
Position
chr11:73,087,444-73,108,519
Genome
hg38
Position
chr11:73,376,399-73,397,474
MIM
611211 OMIM
HGNC
HGNC:13764 HGNC
Ensembl
ENSG00000054967 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 6
Benign 0 16
Likely benign 0 12
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 56
Ranking
ClinVar
0
0
6
80
10
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 :
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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 AI3C
SYNONYM TNFRSF19L
SYNONYM TRLT
MIM 611211 OMIM
HGNC HGNC:13764 HGNC
Ensembl ENSG00000054967 Ensembl
AllianceGenome HGNC:13764
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000393580.2 hg38 chr11 73,376,668 73,396,640 19,973
ENST00000064780.7 hg38 chr11 73,376,399 73,397,474 21,076
ENST00000064780.7 hg19 chr11 73,087,444 73,108,519 21,076
ENST00000393580.2 hg19 chr11 73,087,713 73,107,685 19,973
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