RPL34 ribosomal protein L34

Information
Symbol
RPL34
Type
protein-coding
Description
ribosomal protein L34
Entrez Gene ID
6164
Genome
hg19
Position
chr4:109,541,812-109,551,568
Genome
hg38
Position
chr4:108,620,656-108,630,412
MIM
616862 OMIM
HGNC
HGNC:10340 HGNC
Ensembl
ENSG00000109475 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
12
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
SYNONYM L34
SYNONYM eL34
MIM 616862 OMIM
HGNC HGNC:10340 HGNC
Ensembl ENSG00000109475 Ensembl
AllianceGenome HGNC:10340
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000506397.5 hg38 chr4 108,620,633 108,625,252 4,620
ENST00000394668.2 hg38 chr4 108,620,656 108,630,412 9,757
ENST00000394665.5 hg38 chr4 108,620,590 108,625,255 4,666
ENST00000394667.8 hg38 chr4 108,620,576 108,625,370 4,795
ENST00000502534.5 hg38 chr4 108,620,569 108,625,554 4,986
ENST00000502534.5 hg19 chr4 109,541,725 109,546,710 4,986
ENST00000394667.8 hg19 chr4 109,541,732 109,546,526 4,795
ENST00000394665.5 hg19 chr4 109,541,746 109,546,411 4,666
ENST00000506397.5 hg19 chr4 109,541,789 109,546,408 4,620
ENST00000394668.2 hg19 chr4 109,541,812 109,551,568 9,757
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