FAAP24 FA core complex associated protein 24

Information
Symbol
FAAP24
Type
protein-coding
Description
FA core complex associated protein 24
Entrez Gene ID
91442
Genome
hg19
Position
chr19:33,463,148-33,469,135
Genome
hg38
Position
chr19:32,972,242-32,978,229
MIM
610884 OMIM
HGNC
HGNC:28467 HGNC
Ensembl
ENSG00000131944 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 20
Likely benign 0 10
Uncertain significance 0 26
Ranking
ClinVar
0
0
6
44
4
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 C19orf40
MIM 610884 OMIM
HGNC HGNC:28467 HGNC
Ensembl ENSG00000131944 Ensembl
AllianceGenome HGNC:28467
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000699960.1 hg38 chr19 32,972,257 32,977,074 4,818
ENST00000588258.6 hg38 chr19 32,972,242 32,978,229 5,988
ENST00000589646.5 hg38 chr19 32,972,221 32,976,850 4,630
ENST00000590281.1 hg38 chr19 32,972,304 32,976,812 4,509
ENST00000590179.1 hg38 chr19 32,972,260 32,976,974 4,715
ENST00000589646.5 hg19 chr19 33,463,127 33,467,756 4,630
ENST00000588258.6 hg19 chr19 33,463,148 33,469,135 5,988
ENST00000699960.1 hg19 chr19 33,463,163 33,467,980 4,818
ENST00000590179.1 hg19 chr19 33,463,166 33,467,880 4,715
ENST00000590281.1 hg19 chr19 33,463,210 33,467,718 4,509
Genome browser