SLFN12 schlafen family member 12

Information
Symbol
SLFN12
Type
protein-coding
Description
schlafen family member 12
Entrez Gene ID
55106
Genome
hg19
Position
chr17:33,736,739-33,760,164
Genome
hg38
Position
chr17:35,409,720-35,433,145
MIM
614955 OMIM
HGNC
HGNC:25500 HGNC
Ensembl
ENSG00000172123 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 12
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
70
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 :
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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 SLFN3
MIM 614955 OMIM
HGNC HGNC:25500 HGNC
Ensembl ENSG00000172123 Ensembl
AllianceGenome HGNC:25500
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000714256.1 hg38 chr17 35,411,068 35,432,531 21,464
ENST00000714257.1 hg38 chr17 35,411,069 35,433,475 22,407
ENST00000714254.1 hg38 chr17 35,410,922 35,432,500 21,579
ENST00000714255.1 hg38 chr17 35,410,922 35,432,500 21,579
ENST00000394562.5 hg38 chr17 35,411,060 35,433,196 22,137
ENST00000447040.7 hg38 chr17 35,410,922 35,433,249 22,328
ENST00000445092.6 hg38 chr17 35,409,720 35,433,145 23,426
ENST00000304905.10 hg38 chr17 35,410,922 35,432,500 21,579
ENST00000452764.3 hg38 chr17 35,411,071 35,433,283 22,213
ENST00000445092.6 hg19 chr17 33,736,739 33,760,164 23,426
ENST00000304905.10 hg19 chr17 33,737,941 33,759,519 21,579
ENST00000714254.1 hg19 chr17 33,737,941 33,759,519 21,579
ENST00000714255.1 hg19 chr17 33,737,941 33,759,519 21,579
ENST00000447040.7 hg19 chr17 33,737,941 33,760,268 22,328
ENST00000394562.5 hg19 chr17 33,738,079 33,760,215 22,137
ENST00000714256.1 hg19 chr17 33,738,087 33,759,550 21,464
ENST00000714257.1 hg19 chr17 33,738,088 33,760,494 22,407
ENST00000452764.3 hg19 chr17 33,738,090 33,760,302 22,213
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