EFS embryonal Fyn-associated substrate

Information
Symbol
EFS
Type
protein-coding
Description
embryonal Fyn-associated substrate
Entrez Gene ID
10278
Genome
hg19
Position
chr14:23,825,615-23,834,381
Genome
hg38
Position
chr14:23,356,406-23,365,172
MIM
609906 OMIM
HGNC
HGNC:16898 HGNC
Ensembl
ENSG00000100842 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Uncertain significance 0 100
Ranking
ClinVar
0
0
0
102
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 :
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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 CAS3
SYNONYM CASS3
SYNONYM EFS1
SYNONYM EFS2
SYNONYM HEFS
SYNONYM SIN
MIM 609906 OMIM
HGNC HGNC:16898 HGNC
Ensembl ENSG00000100842 Ensembl
AllianceGenome HGNC:16898
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000351354.3 hg38 chr14 23,356,656 23,365,752 9,097
ENST00000216733.8 hg38 chr14 23,356,406 23,365,172 8,767
ENST00000429593.6 hg38 chr14 23,356,403 23,365,633 9,231
ENST00000429593.6 hg19 chr14 23,825,612 23,834,842 9,231
ENST00000216733.8 hg19 chr14 23,825,615 23,834,381 8,767
ENST00000351354.3 hg19 chr14 23,825,865 23,834,961 9,097
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