BCAP31 B cell receptor associated protein 31

Information
Symbol
BCAP31
Type
protein-coding
Description
B cell receptor associated protein 31
Entrez Gene ID
10134
Genome
hg19
Position
chrX:152,965,947-152,989,521
Genome
hg38
Position
chrX:153,700,492-153,724,066
MIM
300398 OMIM
HGNC
HGNC:16695 HGNC
Ensembl
ENSG00000185825 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 12
Likely pathogenic 0 6
Benign 0 44
Likely benign 0 130
Conflicting classifications of pathogenicity 0 16
no classifications from unflagged records 0 2
not provided 6 2
Uncertain significance 0 112
Ranking
ClinVar
0
0
26
270
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 :
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 6C6-AG
SYNONYM BAP31
SYNONYM CDM
SYNONYM DDCH
SYNONYM DELXQ28
SYNONYM DXS1357E
SYNONYM MICRODELXq28
MIM 300398 OMIM
HGNC HGNC:16695 HGNC
Ensembl ENSG00000185825 Ensembl
AllianceGenome HGNC:16695
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000647529.1 hg38 chrX 153,700,496 153,724,435 23,940
ENST00000458587.8 hg38 chrX 153,700,492 153,724,066 23,575
ENST00000645377.1 hg38 chrX 153,700,497 153,724,388 23,892
ENST00000345046.12 hg38 chrX 153,700,492 153,724,387 23,896
ENST00000458587.8 hg19 chrX 152,965,947 152,989,521 23,575
ENST00000345046.12 hg19 chrX 152,965,947 152,989,842 23,896
ENST00000647529.1 hg19 chrX 152,965,951 152,989,890 23,940
ENST00000645377.1 hg19 chrX 152,965,952 152,989,843 23,892
Genome browser