FANCF FA complementation group F

Information
Symbol
FANCF
Type
protein-coding
Description
FA complementation group F
Entrez Gene ID
2188
Genome
hg19
Position
chr11:22,644,079-22,647,369
Genome
hg38
Position
chr11:22,622,533-22,625,823
MIM
613897 OMIM
HGNC
HGNC:3587 HGNC
Ensembl
ENSG00000183161 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 4 48
Likely pathogenic 0 32
Benign 0 42
Likely benign 0 210
Conflicting classifications of pathogenicity 0 34
not provided 0 8
Uncertain significance 1 524
Ranking
ClinVar
0
0
196
634
8
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 :
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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 FAF
MIM 613897 OMIM
HGNC HGNC:3587 HGNC
Ensembl ENSG00000183161 Ensembl
AllianceGenome HGNC:3587
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000327470.6 hg38 chr11 22,622,533 22,625,823 3,291
ENST00000327470.6 hg19 chr11 22,644,079 22,647,369 3,291
KeyValue
strand-
start22,644,078
Gene SymbolFANCF
Entrez GeneId2,188
Chr Band11p15
end22,647,386
chrchr11
NameFanconi anemia, complementation group F
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