F13B coagulation factor XIII B chain

Information
Symbol
F13B
Type
protein-coding
Description
coagulation factor XIII B chain
Entrez Gene ID
2165
Genome
hg19
Position
chr1:197,007,871-197,036,390
Genome
hg38
Position
chr1:197,038,741-197,067,260
MIM
134580 OMIM
HGNC
HGNC:3534 HGNC
Ensembl
ENSG00000143278 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 16
Likely pathogenic 0 4
Benign 0 36
Likely benign 0 10
Conflicting classifications of pathogenicity 0 24
Uncertain significance 0 130
Ranking
ClinVar
0
0
14
170
10
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 :
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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 FXIIIB
MIM 134580 OMIM
HGNC HGNC:3534 HGNC
Ensembl ENSG00000143278 Ensembl
AllianceGenome HGNC:3534
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000367412.2 hg38 chr1 197,038,741 197,067,260 28,520
ENST00000367412.2 hg19 chr1 197,007,871 197,036,390 28,520
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