MYCBPAP MYCBP associated protein

Information
Symbol
MYCBPAP
Type
protein-coding
Description
MYCBP associated protein
Entrez Gene ID
84073
Genome
hg19
Position
chr17:48,585,800-48,608,862
Genome
hg38
Position
chr17:50,508,439-50,531,501
MIM
609835 OMIM
HGNC
HGNC:19677 HGNC
Ensembl
ENSG00000136449 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 14
Uncertain significance 0 124
Ranking
ClinVar
0
0
0
138
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 AMAP-1
SYNONYM AMAP1
MIM 609835 OMIM
HGNC HGNC:19677 HGNC
Ensembl ENSG00000136449 Ensembl
AllianceGenome HGNC:19677
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000323776.11 hg38 chr17 50,508,439 50,531,501 23,063
ENST00000419930.2 hg38 chr17 50,508,490 50,510,420 1,931
ENST00000323776.11 hg19 chr17 48,585,800 48,608,862 23,063
ENST00000419930.2 hg19 chr17 48,585,851 48,587,781 1,931
Genome browser