RPL27 ribosomal protein L27

Information
Symbol
RPL27
Type
protein-coding
Description
ribosomal protein L27
Entrez Gene ID
6155
Genome
hg19
Position
chr17:41,150,488-41,154,976
Genome
hg38
Position
chr17:42,998,471-43,002,959
MIM
607526 OMIM
HGNC
HGNC:10328 HGNC
Ensembl
ENSG00000131469 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 24
Likely benign 0 20
Uncertain significance 0 48
Ranking
ClinVar
0
0
14
76
2
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
SYNONYM DBA16
SYNONYM L27
SYNONYM eL27
MIM 607526 OMIM
HGNC HGNC:10328 HGNC
Ensembl ENSG00000131469 Ensembl
AllianceGenome HGNC:10328
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000589037.5 hg38 chr17 42,998,273 43,002,949 4,677
ENST00000589913.6 hg38 chr17 42,998,471 43,002,959 4,489
ENST00000253788.12 hg38 chr17 42,998,419 43,002,959 4,541
ENST00000589037.5 hg19 chr17 41,150,290 41,154,966 4,677
ENST00000253788.12 hg19 chr17 41,150,436 41,154,976 4,541
ENST00000589913.6 hg19 chr17 41,150,488 41,154,976 4,489
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