SAA2-SAA4 SAA2-SAA4 readthrough

Information
Symbol
SAA2-SAA4
Type
protein-coding
Description
SAA2-SAA4 readthrough
Entrez Gene ID
100528017
Genome
hg19
Position
chr11:18,252,970-18,270,182
Genome
hg38
Position
chr11:18,231,423-18,248,635
HGNC
HGNC:39550 HGNC
Ensembl
ENSG00000255071 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
2
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:39550 HGNC
Ensembl ENSG00000255071 Ensembl
AllianceGenome HGNC:39550
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000524555.3 hg38 chr11 18,231,423 18,248,635 17,213
ENST00000524555.3 hg19 chr11 18,252,970 18,270,182 17,213
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