RNF212B ring finger protein 212B

Information
Symbol
RNF212B
Type
protein-coding
Description
ring finger protein 212B
Entrez Gene ID
100507650
Genome
hg19
Position
chr14:23,654,525-23,742,614
Genome
hg38
Position
chr14:23,185,316-23,273,405
HGNC
HGNC:20438 HGNC
Ensembl
ENSG00000215277 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Ranking
ClinVar
0
0
0
2
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 :
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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 C14orf164
HGNC HGNC:20438 HGNC
Ensembl ENSG00000215277 Ensembl
AllianceGenome HGNC:20438
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000430154.7 hg38 chr14 23,237,936 23,273,477 35,542
ENST00000399910.5 hg38 chr14 23,185,316 23,273,405 88,090
ENST00000399905.5 hg38 chr14 23,258,485 23,273,477 14,993
ENST00000399910.5 hg19 chr14 23,654,525 23,742,614 88,090
ENST00000430154.7 hg19 chr14 23,707,145 23,742,686 35,542
ENST00000399905.5 hg19 chr14 23,727,694 23,742,686 14,993
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