F10 coagulation factor X

Information
Symbol
F10
Type
protein-coding
Description
coagulation factor X
Entrez Gene ID
2159
Genome
hg19
Position
chr13:113,777,113-113,803,843
Genome
hg38
Position
chr13:113,122,799-113,149,529
MIM
613872 OMIM
HGNC
HGNC:3528 HGNC
Ensembl
ENSG00000126218 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 22
Likely pathogenic 0 44
Benign 0 42
Likely benign 0 16
Conflicting classifications of pathogenicity 0 18
Uncertain significance 0 102
Ranking
ClinVar
0
0
32
160
26
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 FX
SYNONYM FXA
MIM 613872 OMIM
HGNC HGNC:3528 HGNC
Ensembl ENSG00000126218 Ensembl
AllianceGenome HGNC:3528
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000375551.7 hg38 chr13 113,122,814 113,149,527 26,714
ENST00000375559.8 hg38 chr13 113,122,799 113,149,529 26,731
ENST00000409306.5 hg38 chr13 113,122,814 113,149,462 26,649
ENST00000375559.8 hg19 chr13 113,777,113 113,803,843 26,731
ENST00000409306.5 hg19 chr13 113,777,128 113,803,776 26,649
ENST00000375551.7 hg19 chr13 113,777,128 113,803,841 26,714
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