LOC112694756 uncharaterized LOC112694756

Information
Symbol
LOC112694756
Type
protein-coding
Description
uncharaterized LOC112694756
Entrez Gene ID
112694756
Genome
hg19
Position
chr16:30,064,472-30,081,735
Genome
hg38
Position
chr16:30,053,151-30,070,414
Ensembl
ENSG00000285043 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 8
Benign 0 32
Likely benign 0 246
Conflicting classifications of pathogenicity 0 22
Uncertain significance 0 236
Ranking
ClinVar
0
0
92
420
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
SYNONYM ALDA
SYNONYM ALDOA
Ensembl ENSG00000285043 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000568435.6 hg38 chr16 30,053,134 30,067,290 14,157
ENST00000338110.11 hg38 chr16 30,053,151 30,070,414 17,264
ENST00000566897.6 hg38 chr16 30,053,127 30,070,413 17,287
ENST00000395248.6 hg38 chr16 30,053,123 30,070,403 17,281
ENST00000562240.1 hg38 chr16 30,053,160 30,064,038 10,879
ENST00000575627.5 hg38 chr16 30,053,127 30,063,928 10,802
ENST00000395248.6 hg19 chr16 30,064,444 30,081,724 17,281
ENST00000575627.5 hg19 chr16 30,064,448 30,075,249 10,802
ENST00000566897.6 hg19 chr16 30,064,448 30,081,734 17,287
ENST00000568435.6 hg19 chr16 30,064,455 30,078,611 14,157
ENST00000338110.11 hg19 chr16 30,064,472 30,081,735 17,264
ENST00000562240.1 hg19 chr16 30,064,481 30,075,359 10,879
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