RELA RELA proto-oncogene, NF-kB subunit

Information
Symbol
RELA
Type
protein-coding
Description
RELA proto-oncogene, NF-kB subunit
Entrez Gene ID
5970
Genome
hg19
Position
chr11:65,421,072-65,430,387
Genome
hg38
Position
chr11:65,653,601-65,662,916
MIM
164014 OMIM
HGNC
HGNC:9955 HGNC
Ensembl
ENSG00000173039 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 40
Likely pathogenic 0 16
Benign 0 36
Likely benign 0 332
Conflicting classifications of pathogenicity 0 12
Uncertain significance 0 296
Ranking
ClinVar
0
0
54
648
6
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 AIF3BL3
SYNONYM CMCU
SYNONYM NFKB3
SYNONYM p65
MIM 164014 OMIM
HGNC HGNC:9955 HGNC
Ensembl ENSG00000173039 Ensembl
AllianceGenome HGNC:9955
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000406246.8 hg38 chr11 65,653,601 65,662,916 9,316
ENST00000612991.4 hg38 chr11 65,653,599 65,662,972 9,374
ENST00000308639.13 hg38 chr11 65,653,602 65,663,090 9,489
ENST00000525693.5 hg38 chr11 65,653,601 65,662,895 9,295
ENST00000525693.5 hg19 chr11 65,421,072 65,430,366 9,295
ENST00000406246.8 hg19 chr11 65,421,072 65,430,387 9,316
ENST00000308639.13 hg19 chr11 65,421,073 65,430,561 9,489
ENST00000612991.4 hg19 chr11 65,421,070 65,430,443 9,374
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