SIRT6 sirtuin 6

Information
Symbol
SIRT6
Type
protein-coding
Description
sirtuin 6
Entrez Gene ID
51548
Genome
hg19
Position
chr19:4,174,106-4,182,560
Genome
hg38
Position
chr19:4,174,109-4,182,563
MIM
606211 OMIM
HGNC
HGNC:14934 HGNC
Ensembl
ENSG00000077463 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 4
Likely benign 0 12
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
68
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 SIR2L6
SYNONYM hSIRT6
MIM 606211 OMIM
HGNC HGNC:14934 HGNC
Ensembl ENSG00000077463 Ensembl
AllianceGenome HGNC:14934
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000601488.5 hg38 chr19 4,174,109 4,182,547 8,439
ENST00000305232.10 hg38 chr19 4,174,109 4,182,550 8,442
ENST00000337491.7 hg38 chr19 4,174,109 4,182,563 8,455
ENST00000594279.5 hg38 chr19 4,174,141 4,182,279 8,139
ENST00000601488.5 hg19 chr19 4,174,106 4,182,544 8,439
ENST00000305232.10 hg19 chr19 4,174,106 4,182,547 8,442
ENST00000337491.7 hg19 chr19 4,174,106 4,182,560 8,455
ENST00000594279.5 hg19 chr19 4,174,138 4,182,276 8,139
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