NBPF11 NBPF member 11

Information
Symbol
NBPF11
Type
protein-coding
Description
NBPF member 11
Entrez Gene ID
200030
Genome
hg38
Position
chr1:148,102,151-148,152,322
MIM
614001 OMIM
HGNC
HGNC:31993 HGNC
Ensembl
ENSG00000263956 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 4 0
Uncertain significance 0 1
Ranking
ClinVar
0
0
0
5
0
Frequency
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 NBPF24
MIM 614001 OMIM
HGNC HGNC:31993 HGNC
Ensembl ENSG00000263956 Ensembl
AllianceGenome HGNC:31993
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000615281.4 hg38 chr1 148,102,151 148,152,322 50,172
ENST00000682118.1 hg38 chr1 148,102,151 148,152,281 50,131
ENST00000614015.4 hg38 chr1 148,102,047 148,127,288 25,242
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