C18orf32 chromosome 18 open reading frame 32

Information
Symbol
C18orf32
Type
protein-coding
Description
chromosome 18 open reading frame 32
Entrez Gene ID
497661
Genome
hg19
Position
chr18:47,003,613-47,013,604
Genome
hg38
Position
chr18:49,477,243-49,487,234
MIM
619979 OMIM
HGNC
HGNC:31690 HGNC
Ensembl
ENSG00000177576 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
6
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 :
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
SYNONYM GPIBD25
MIM 619979 OMIM
HGNC HGNC:31690 HGNC
Ensembl ENSG00000177576 Ensembl
AllianceGenome HGNC:31690
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000582392.2 hg38 chr18 49,482,066 49,486,613 4,548
ENST00000613385.4 hg38 chr18 49,477,250 49,487,252 10,003
ENST00000318240.8 hg38 chr18 49,477,243 49,487,234 9,992
ENST00000318240.8 hg19 chr18 47,003,613 47,013,604 9,992
ENST00000613385.4 hg19 chr18 47,003,620 47,013,622 10,003
ENST00000582392.2 hg19 chr18 47,008,436 47,012,983 4,548
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