SLFN14 schlafen family member 14

Information
Symbol
SLFN14
Type
protein-coding
Description
schlafen family member 14
Entrez Gene ID
342618
Genome
hg19
Position
chr17:33,871,004-33,887,838
Genome
hg38
Position
chr17:35,543,985-35,560,819
MIM
614958 OMIM
HGNC
HGNC:32689 HGNC
Ensembl
ENSG00000236320 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 4
Benign 0 50
Likely benign 0 24
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 130
Ranking
ClinVar
0
0
32
156
18
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 :
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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 BDPLT20
MIM 614958 OMIM
HGNC HGNC:32689 HGNC
Ensembl ENSG00000236320 Ensembl
AllianceGenome HGNC:32689
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000674182.1 hg38 chr17 35,543,985 35,560,819 16,835
ENST00000415846.3 hg38 chr17 35,548,125 35,558,098 9,974
ENST00000674182.1 hg19 chr17 33,871,004 33,887,838 16,835
ENST00000415846.3 hg19 chr17 33,875,144 33,885,117 9,974
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