RNF148 ring finger protein 148

Information
Symbol
RNF148
Type
protein-coding
Description
ring finger protein 148
Entrez Gene ID
378925
Genome
hg19
Position
chr7:122,341,722-122,342,976
Genome
hg38
Position
chr7:122,701,668-122,702,922
HGNC
HGNC:22411 HGNC
Ensembl
ENSG00000235631 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 56
Ranking
ClinVar
0
0
0
60
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 :
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:22411 HGNC
Ensembl ENSG00000235631 Ensembl
AllianceGenome HGNC:22411
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000434824.2 hg38 chr7 122,701,668 122,702,922 1,255
ENST00000447240.1 hg38 chr7 122,701,670 122,702,912 1,243
ENST00000434824.2 hg19 chr7 122,341,722 122,342,976 1,255
ENST00000447240.1 hg19 chr7 122,341,724 122,342,966 1,243
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