ZNF674 zinc finger protein 674

Information
Symbol
ZNF674
Type
protein-coding
Description
zinc finger protein 674
Entrez Gene ID
641339
Genome
hg19
Position
chrX:46,357,162-46,404,876
Genome
hg38
Position
chrX:46,497,727-46,545,441
MIM
300573 OMIM
HGNC
HGNC:17625 HGNC
Ensembl
ENSG00000251192 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 16
Conflicting classifications of pathogenicity 0 4
not provided 6 0
Uncertain significance 0 50
Ranking
ClinVar
0
0
8
62
6
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 MRX92
SYNONYM ZNF673B
MIM 300573 OMIM
HGNC HGNC:17625 HGNC
Ensembl ENSG00000251192 Ensembl
AllianceGenome HGNC:17625
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000414387.6 hg38 chrX 46,499,437 46,544,611 45,175
ENST00000683375.1 hg38 chrX 46,497,725 46,545,421 47,697
ENST00000523374.5 hg38 chrX 46,497,727 46,545,441 47,715
ENST00000683375.1 hg19 chrX 46,357,160 46,404,856 47,697
ENST00000523374.5 hg19 chrX 46,357,162 46,404,876 47,715
ENST00000414387.6 hg19 chrX 46,358,872 46,404,046 45,175
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