LY6G6F-LY6G6D LY6G6F-LY6G6D readthrough

Information
Symbol
LY6G6F-LY6G6D
Type
protein-coding
Description
LY6G6F-LY6G6D readthrough
Entrez Gene ID
110599563
Genome
hg19
Position
chr6:31,674,681-31,685,695
Genome
hg38
Position
chr6:31,706,904-31,717,918
HGNC
HGNC:38821 HGNC
Ensembl
ENSG00000250641 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
not provided 6 0
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
50
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
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 G6F-LY6G6D
SYNONYM MEGT-1
SYNONYM MEGT1
HGNC HGNC:38821 HGNC
Ensembl ENSG00000250641 Ensembl
AllianceGenome HGNC:38821
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000503322.1 hg38 chr6 31,706,904 31,717,918 11,015
ENST00000503322.1 hg19 chr6 31,674,681 31,685,695 11,015
Genome browser