LOC128706666 uncharacterized LOC128706666

Information
Symbol
LOC128706666
Type
protein-coding
Description
uncharacterized LOC128706666
Entrez Gene ID
128706666
Genome
hg19
Position
chr20:10,394,168-10,412,570
Genome
hg38
Position
chr20:10,413,520-10,431,922
Ensembl
ENSG00000285508 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 8
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 36
Ranking
ClinVar
0
0
2
44
4
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 ENSG00000285508 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000609375.1 hg38 chr20 10,413,520 10,431,922 18,403
ENST00000713549.1 hg38 chr20 10,413,708 10,434,222 20,515
ENST00000609375.1 hg19 chr20 10,394,168 10,412,570 18,403
ENST00000713549.1 hg19 chr20 10,394,356 10,414,870 20,515
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