TMA7B translation machinery associated 7 homolog B

Information
Symbol
TMA7B
Type
protein-coding
Description
translation machinery associated 7 homolog B
Entrez Gene ID
112268293
Genome
hg19
Position
chr22:40,356,401-40,360,909
Genome
hg38
Position
chr22:39,960,397-39,964,905
HGNC
HGNC:53893 HGNC
Ensembl
ENSG00000225528 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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 :
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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:53893 HGNC
Ensembl ENSG00000225528 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000424496.3 hg38 chr22 39,960,397 39,964,905 4,509
ENST00000424496.3 hg19 chr22 40,356,401 40,360,909 4,509
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