SLC22A31 solute carrier family 22 member 31

Information
Symbol
SLC22A31
Type
protein-coding
Description
solute carrier family 22 member 31
Entrez Gene ID
146429
Genome
hg19
Position
chr16:89,262,169-89,266,945
Genome
hg38
Position
chr16:89,195,761-89,200,537
HGNC
HGNC:27091 HGNC
Ensembl
ENSG00000259803 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 4
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
64
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 :
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
HGNC HGNC:27091 HGNC
Ensembl ENSG00000259803 Ensembl
AllianceGenome HGNC:27091
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000562855.7 hg38 chr16 89,195,761 89,201,651 5,891
ENST00000614943.4 hg38 chr16 89,195,761 89,200,121 4,361
ENST00000682282.1 hg38 chr16 89,195,761 89,200,537 4,777
ENST00000614943.4 hg19 chr16 89,262,169 89,266,529 4,361
ENST00000682282.1 hg19 chr16 89,262,169 89,266,945 4,777
ENST00000562855.7 hg19 chr16 89,262,169 89,268,059 5,891
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