RNF157 ring finger protein 157

Information
Symbol
RNF157
Type
protein-coding
Description
ring finger protein 157
Entrez Gene ID
114804
Genome
hg19
Position
chr17:74,138,555-74,236,574
Genome
hg38
Position
chr17:76,142,474-76,240,493
HGNC
HGNC:29402 HGNC
Ensembl
ENSG00000141576 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 2
Uncertain significance 0 56
Ranking
ClinVar
0
0
0
66
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:29402 HGNC
Ensembl ENSG00000141576 Ensembl
AllianceGenome HGNC:29402
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000319945.10 hg38 chr17 76,144,340 76,240,308 95,969
ENST00000269391.11 hg38 chr17 76,142,474 76,240,493 98,020
ENST00000647930.1 hg38 chr17 76,142,465 76,240,289 97,825
ENST00000592271.1 hg38 chr17 76,211,877 76,240,301 28,425
ENST00000647930.1 hg19 chr17 74,138,546 74,236,370 97,825
ENST00000269391.11 hg19 chr17 74,138,555 74,236,574 98,020
ENST00000319945.10 hg19 chr17 74,140,421 74,236,389 95,969
ENST00000592271.1 hg19 chr17 74,207,958 74,236,382 28,425
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