RAP2C-AS1 RAP2C antisense RNA 1

Information
Symbol
RAP2C-AS1
Type
ncRNA
Description
RAP2C antisense RNA 1
Entrez Gene ID
101928578
Genome
hg19
Position
chrX:131,352,237-131,566,890
Genome
hg38
Position
chrX:132,218,209-132,432,862
HGNC
HGNC:40957 HGNC
Ensembl
ENSG00000232160 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:40957 HGNC
Ensembl ENSG00000232160 Ensembl
AllianceGenome HGNC:40957
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000441399.3 hg38 chrX 132,218,209 132,432,862 214,654
ENST00000669125.1 hg38 chrX 132,218,499 132,241,642 23,144
ENST00000441399.3 hg19 chrX 131,352,237 131,566,890 214,654
ENST00000669125.1 hg19 chrX 131,352,527 131,375,670 23,144
Genome browser