ZCCHC12 zinc finger CCHC-type containing 12

Information
Symbol
ZCCHC12
Type
protein-coding
Description
zinc finger CCHC-type containing 12
Entrez Gene ID
170261
Genome
hg19
Position
chrX:117,957,787-117,960,931
Genome
hg38
Position
chrX:118,823,824-118,826,968
MIM
300701 OMIM
HGNC
HGNC:27273 HGNC
Ensembl
ENSG00000174460 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 4
Conflicting classifications of pathogenicity 0 4
not provided 6 0
Uncertain significance 0 26
Ranking
ClinVar
0
0
2
34
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
SYNONYM PNMA7A
SYNONYM SIZN
SYNONYM SIZN1
MIM 300701 OMIM
HGNC HGNC:27273 HGNC
Ensembl ENSG00000174460 Ensembl
AllianceGenome HGNC:27273
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000310164.3 hg38 chrX 118,823,824 118,826,968 3,145
ENST00000310164.3 hg19 chrX 117,957,787 117,960,931 3,145
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