FAM78B family with sequence similarity 78 member B

Information
Symbol
FAM78B
Type
protein-coding
Description
family with sequence similarity 78 member B
Entrez Gene ID
149297
Genome
hg19
Position
chr1:166,038,536-166,136,238
Genome
hg38
Position
chr1:166,069,299-166,167,001
HGNC
HGNC:13495 HGNC
Ensembl
ENSG00000188859 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
16
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
HGNC HGNC:13495 HGNC
Ensembl ENSG00000188859 Ensembl
AllianceGenome HGNC:13495
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000338353.4 hg38 chr1 166,070,020 166,166,969 96,950
ENST00000354422.4 hg38 chr1 166,069,299 166,167,001 97,703
ENST00000354422.4 hg19 chr1 166,038,536 166,136,238 97,703
ENST00000338353.4 hg19 chr1 166,039,257 166,136,206 96,950
Genome browser