LOC128125816 uncharacterized LOC128125816

Information
Symbol
LOC128125816
Type
protein-coding
Description
uncharacterized LOC128125816
Entrez Gene ID
128125816
Genome
hg19
Position
chr12:122,692,209-122,712,081
Genome
hg38
Position
chr12:122,207,662-122,227,534
Ensembl
ENSG00000284934 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 46
Likely benign 0 82
Conflicting classifications of pathogenicity 0 20
not provided 0 2
Uncertain significance 0 76
Ranking
ClinVar
0
0
26
168
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 ENSG00000284934 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000645606.1 hg38 chr12 122,207,662 122,227,534 19,873
ENST00000713558.1 hg38 chr12 122,226,430 122,226,564 135
ENST00000475784.1 hg38 chr12 122,226,216 122,227,533 1,318
ENST00000645606.1 hg19 chr12 122,692,209 122,712,081 19,873
ENST00000475784.1 hg19 chr12 122,710,763 122,712,080 1,318
ENST00000713558.1 hg19 chr12 122,710,977 122,711,111 135
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