RNF214 ring finger protein 214

Information
Symbol
RNF214
Type
protein-coding
Description
ring finger protein 214
Entrez Gene ID
257160
Genome
hg19
Position
chr11:117,103,387-117,157,170
Genome
hg38
Position
chr11:117,232,671-117,286,454
HGNC
HGNC:25335 HGNC
Ensembl
ENSG00000167257 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 2 0
Likely benign 0 4
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
56
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
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
HGNC HGNC:25335 HGNC
Ensembl ENSG00000167257 Ensembl
AllianceGenome HGNC:25335
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000531452.5 hg38 chr11 117,232,736 117,285,688 52,953
ENST00000531287.5 hg38 chr11 117,232,736 117,285,164 52,429
ENST00000300650.9 hg38 chr11 117,232,671 117,286,454 53,784
ENST00000530849.1 hg38 chr11 117,234,263 117,286,445 52,183
ENST00000300650.9 hg19 chr11 117,103,387 117,157,170 53,784
ENST00000531287.5 hg19 chr11 117,103,452 117,155,880 52,429
ENST00000531452.5 hg19 chr11 117,103,452 117,156,404 52,953
ENST00000530849.1 hg19 chr11 117,104,979 117,157,161 52,183
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