FAM90A22 family with sequence similarity 90 member A22

Information
Symbol
FAM90A22
Type
protein-coding
Description
family with sequence similarity 90 member A22
Entrez Gene ID
645558
Genome
hg19
Position
chr8:7,429,517-7,432,528
Genome
hg38
Position
chr8:7,571,995-7,575,006
HGNC
HGNC:32270 HGNC
Ensembl
ENSG00000285687 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
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
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 FAM90A22P
HGNC HGNC:32270 HGNC
Ensembl ENSG00000285687 Ensembl
AllianceGenome HGNC:32270
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000648590.1 hg38 chr8 7,571,995 7,575,006 3,012
ENST00000648590.1 hg19 chr8 7,429,517 7,432,528 3,012
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