MCM7 minichromosome maintenance complex component 7

Information
Symbol
MCM7
Type
protein-coding
Description
minichromosome maintenance complex component 7
Entrez Gene ID
4176
Genome
hg19
Position
chr7:99,690,351-99,699,020
Genome
hg38
Position
chr7:100,092,728-100,101,397
MIM
600592 OMIM
HGNC
HGNC:6950 HGNC
Ensembl
ENSG00000166508 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 18
Likely pathogenic 0 10
Benign 0 20
Likely benign 0 42
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 160
Ranking
ClinVar
0
0
14
230
2
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 CDC47
SYNONYM MCM2
SYNONYM P1.1-MCM3
SYNONYM P1CDC47
SYNONYM P85MCM
SYNONYM PNAS146
SYNONYM PPP1R104
MIM 600592 OMIM
HGNC HGNC:6950 HGNC
Ensembl ENSG00000166508 Ensembl
AllianceGenome HGNC:6950
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000425308.6 hg38 chr7 100,092,728 100,100,869 8,142
ENST00000343023.10 hg38 chr7 100,092,780 100,101,940 9,161
ENST00000303887.10 hg38 chr7 100,092,728 100,101,397 8,670
ENST00000710813.1 hg38 chr7 100,092,233 100,100,743 8,511
ENST00000710815.1 hg38 chr7 100,092,751 100,100,740 7,990
ENST00000710813.1 hg19 chr7 99,689,856 99,698,366 8,511
ENST00000425308.6 hg19 chr7 99,690,351 99,698,492 8,142
ENST00000303887.10 hg19 chr7 99,690,351 99,699,020 8,670
ENST00000710815.1 hg19 chr7 99,690,374 99,698,363 7,990
ENST00000343023.10 hg19 chr7 99,690,403 99,699,563 9,161
Genome browser