EPPIN-WFDC6 EPPIN-WFDC6 readthrough

Information
Symbol
EPPIN-WFDC6
Type
protein-coding
Description
EPPIN-WFDC6 readthrough
Entrez Gene ID
100526773
Genome
hg19
Position
chr20:44,162,835-44,176,301
Genome
hg38
Position
chr20:45,534,196-45,547,662
HGNC
HGNC:38825 HGNC
Ensembl
ENSG00000249139 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 1 0
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
18
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 SPINLW1-WFDC6
HGNC HGNC:38825 HGNC
Ensembl ENSG00000249139 Ensembl
AllianceGenome HGNC:38825
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000504988.1 hg38 chr20 45,536,986 45,547,426 10,441
ENST00000651288.1 hg38 chr20 45,534,196 45,547,662 13,467
ENST00000651288.1 hg19 chr20 44,162,835 44,176,301 13,467
ENST00000504988.1 hg19 chr20 44,165,625 44,176,065 10,441
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