SLC9A3P2 solute carrier family 9 member 3 pseudogene 2

Information
Symbol
SLC9A3P2
Type
pseudo
Description
solute carrier family 9 member 3 pseudogene 2
Entrez Gene ID
128997
Genome
hg19
Position
chr22:21,007,017-21,009,037
Genome
hg38
Position
chr22:20,652,730-20,654,750
HGNC
HGNC:19325 HGNC
Ensembl
ENSG00000238125 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 15 0
Ranking
ClinVar
0
0
0
0
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
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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:19325 HGNC
Ensembl ENSG00000238125 Ensembl
AllianceGenome HGNC:19325
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000447821.1 hg38 chr22 20,652,730 20,654,750 2,021
ENST00000447821.1 hg19 chr22 21,007,017 21,009,037 2,021
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