ABCF1 ATP binding cassette subfamily F member 1

Information
Symbol
ABCF1
Type
protein-coding
Description
ATP binding cassette subfamily F member 1
Entrez Gene ID
23
Genome
hg19
Position
chr6:30,539,219-30,559,299
Genome
hg38
Position
chr6:30,571,442-30,591,522
MIM
603429 OMIM
HGNC
HGNC:70 HGNC
Ensembl
ENSG00000204574 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 8
not provided 17 0
Uncertain significance 0 76
Ranking
ClinVar
0
0
0
86
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
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 ABC27
SYNONYM ABC50
MIM 603429 OMIM
HGNC HGNC:70 HGNC
Ensembl ENSG00000204574 Ensembl
AllianceGenome HGNC:70
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000376545.7 hg38 chr6 30,571,393 30,591,313 19,921
ENST00000441867.6 hg38 chr6 30,571,424 30,591,522 20,099
ENST00000326195.13 hg38 chr6 30,571,442 30,591,522 20,081
ENST00000376545.7 hg19 chr6 30,539,170 30,559,090 19,921
ENST00000441867.6 hg19 chr6 30,539,201 30,559,299 20,099
ENST00000326195.13 hg19 chr6 30,539,219 30,559,299 20,081
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