SLFN12L schlafen family member 12 like

Information
Symbol
SLFN12L
Type
protein-coding
Description
schlafen family member 12 like
Entrez Gene ID
100506736
Genome
hg19
Position
chr17:33,791,273-33,864,697
Genome
hg38
Position
chr17:35,464,254-35,537,678
MIM
614956 OMIM
HGNC
HGNC:33920 HGNC
Ensembl
ENSG00000205045 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
Uncertain significance 0 48
Ranking
ClinVar
0
0
0
56
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
MIM 614956 OMIM
HGNC HGNC:33920 HGNC
Ensembl ENSG00000205045 Ensembl
AllianceGenome HGNC:33920
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000628453.4 hg38 chr17 35,464,254 35,537,678 73,425
ENST00000260908.13 hg38 chr17 35,464,254 35,487,857 23,604
ENST00000260908.13 hg19 chr17 33,791,273 33,814,876 23,604
ENST00000628453.4 hg19 chr17 33,791,273 33,864,697 73,425
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