RNF151 ring finger protein 151

Information
Symbol
RNF151
Type
protein-coding
Description
ring finger protein 151
Entrez Gene ID
146310
Genome
hg19
Position
chr16:2,016,857-2,018,950
Genome
hg38
Position
chr16:1,966,856-1,968,949
HGNC
HGNC:23235 HGNC
Ensembl
ENSG00000179580 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
52
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 :
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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
HGNC HGNC:23235 HGNC
Ensembl ENSG00000179580 Ensembl
AllianceGenome HGNC:23235
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000569714.6 hg38 chr16 1,966,856 1,968,949 2,094
ENST00000321392.4 hg38 chr16 1,967,273 1,968,975 1,703
ENST00000569210.6 hg38 chr16 1,966,823 1,968,948 2,126
ENST00000569210.6 hg19 chr16 2,016,824 2,018,949 2,126
ENST00000569714.6 hg19 chr16 2,016,857 2,018,950 2,094
ENST00000321392.4 hg19 chr16 2,017,274 2,018,976 1,703
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