XRCC6P5 X-ray repair cross complementing 6 pseudogene 5

Information
Symbol
XRCC6P5
Type
pseudo
Description
X-ray repair cross complementing 6 pseudogene 5
Entrez Gene ID
442459
Genome
hg19
Position
chrX:98,974,362-98,976,156
Genome
hg38
Position
chrX:99,719,364-99,721,158
HGNC
HGNC:45187 HGNC
Ensembl
ENSG00000215070 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 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:45187 HGNC
Ensembl ENSG00000215070 Ensembl
AllianceGenome HGNC:45187
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000435236.2 hg38 chrX 99,719,364 99,721,158 1,795
ENST00000435236.2 hg19 chrX 98,974,362 98,976,156 1,795
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