OAF out at first homolog

Information
Symbol
OAF
Type
protein-coding
Description
out at first homolog
Entrez Gene ID
220323
Genome
hg19
Position
chr11:120,081,740-120,101,043
Genome
hg38
Position
chr11:120,211,032-120,230,334
HGNC
HGNC:28752 HGNC
Ensembl
ENSG00000184232 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
40
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 NS5ATP13TP2
HGNC HGNC:28752 HGNC
Ensembl ENSG00000184232 Ensembl
AllianceGenome HGNC:28752
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000328965.9 hg38 chr11 120,211,032 120,230,334 19,303
ENST00000531220.1 hg38 chr11 120,211,301 120,229,240 17,940
ENST00000328965.9 hg19 chr11 120,081,740 120,101,043 19,304
ENST00000531220.1 hg19 chr11 120,082,009 120,099,949 17,941
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