LOC101059915 chromosome X open reading frame 49-like

Information
Symbol
LOC101059915
Type
protein-coding
Description
chromosome X open reading frame 49-like
Entrez Gene ID
101059915
Genome
hg19
Position
chrX:70,887,396-70,891,377
Genome
hg38
Position
chrX:71,667,546-71,671,527
Ensembl
ENSG00000283599 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Ranking
ClinVar
0
0
0
8
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
Ensembl ENSG00000283599 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000636797.3 hg38 chrX 71,667,542 71,671,524 3,983
ENST00000636096.3 hg38 chrX 71,667,546 71,671,527 3,982
ENST00000636797.3 hg19 chrX 70,887,392 70,891,374 3,983
ENST00000636096.3 hg19 chrX 70,887,396 70,891,377 3,982
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