SLFN13 schlafen family member 13

Information
Symbol
SLFN13
Type
protein-coding
Description
schlafen family member 13
Entrez Gene ID
146857
Genome
hg19
Position
chr17:33,762,115-33,775,785
Genome
hg38
Position
chr17:35,435,096-35,448,766
MIM
614957 OMIM
HGNC
HGNC:26481 HGNC
Ensembl
ENSG00000154760 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 22
Uncertain significance 0 128
Ranking
ClinVar
0
0
0
156
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
SYNONYM SLFN10
SYNONYM hSLFN13
MIM 614957 OMIM
HGNC HGNC:26481 HGNC
Ensembl ENSG00000154760 Ensembl
AllianceGenome HGNC:26481
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000534689.5 hg38 chr17 35,439,480 35,448,764 9,285
ENST00000285013.11 hg38 chr17 35,435,096 35,448,766 13,671
ENST00000542635.5 hg38 chr17 35,437,545 35,447,394 9,850
ENST00000533791.5 hg38 chr17 35,439,498 35,446,010 6,513
ENST00000526861.5 hg38 chr17 35,437,543 35,448,782 11,240
ENST00000285013.11 hg19 chr17 33,762,115 33,775,785 13,671
ENST00000526861.5 hg19 chr17 33,764,562 33,775,801 11,240
ENST00000542635.5 hg19 chr17 33,764,564 33,774,413 9,850
ENST00000534689.5 hg19 chr17 33,766,499 33,775,783 9,285
ENST00000533791.5 hg19 chr17 33,766,517 33,773,029 6,513
Genome browser