SLFN11 schlafen family member 11

Information
Symbol
SLFN11
Type
protein-coding
Description
schlafen family member 11
Entrez Gene ID
91607
Genome
hg19
Position
chr17:33,677,324-33,700,640
Genome
hg38
Position
chr17:35,350,305-35,373,621
MIM
614953 OMIM
HGNC
HGNC:26633 HGNC
Ensembl
ENSG00000172716 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 6
Likely benign 0 24
Uncertain significance 0 110
Ranking
ClinVar
0
0
0
140
2
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 SLFN8/9
MIM 614953 OMIM
HGNC HGNC:26633 HGNC
Ensembl ENSG00000172716 Ensembl
AllianceGenome HGNC:26633
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000308377.8 hg38 chr17 35,350,305 35,373,607 23,303
ENST00000394566.5 hg38 chr17 35,350,305 35,373,620 23,316
ENST00000685675.1 hg38 chr17 35,350,305 35,373,621 23,317
ENST00000308377.8 hg19 chr17 33,677,324 33,700,626 23,303
ENST00000394566.5 hg19 chr17 33,677,324 33,700,639 23,316
ENST00000685675.1 hg19 chr17 33,677,324 33,700,640 23,317
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