LOC122526780 uncharacterized LOC122526780

Information
Symbol
LOC122526780
Type
protein-coding
Description
uncharacterized LOC122526780
Entrez Gene ID
122526780
Genome
hg19
Position
chr17:6,481,467-6,544,031
Genome
hg38
Position
chr17:6,578,147-6,640,711
Ensembl
ENSG00000282936 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 46
Likely pathogenic 0 28
Benign 0 124
Likely benign 0 278
Conflicting classifications of pathogenicity 0 12
Uncertain significance 0 348
Ranking
ClinVar
0
0
128
662
8
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 ENSG00000282936 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000634965.3 hg38 chr17 6,578,147 6,640,711 62,565
ENST00000713584.1 hg38 chr17 6,636,780 6,640,316 3,537
ENST00000634965.3 hg19 chr17 6,481,467 6,544,031 62,565
ENST00000713584.1 hg19 chr17 6,540,100 6,543,636 3,537
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