BPIFC BPI fold containing family C

Information
Symbol
BPIFC
Type
protein-coding
Description
BPI fold containing family C
Entrez Gene ID
254240
Genome
hg19
Position
chr22:32,809,832-32,860,433
Genome
hg38
Position
chr22:32,413,845-32,464,446
MIM
614109 OMIM
HGNC
HGNC:16503 HGNC
Ensembl
ENSG00000184459 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 2
Uncertain significance 0 28
Ranking
ClinVar
0
0
0
36
0
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 BPIL2
MIM 614109 OMIM
HGNC HGNC:16503 HGNC
Ensembl ENSG00000184459 Ensembl
AllianceGenome HGNC:16503
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000397452.5 hg38 chr22 32,413,847 32,464,484 50,638
ENST00000397450.2 hg38 chr22 32,453,334 32,464,449 11,116
ENST00000300399.9 hg38 chr22 32,413,845 32,464,446 50,602
ENST00000300399.9 hg19 chr22 32,809,832 32,860,433 50,602
ENST00000397452.5 hg19 chr22 32,809,834 32,860,471 50,638
ENST00000397450.2 hg19 chr22 32,849,321 32,860,436 11,116
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