FAM156B family with sequence similarity 156 member B

Information
Symbol
FAM156B
Type
protein-coding
Description
family with sequence similarity 156 member B
Entrez Gene ID
727866
Genome
hg19
Position
chrX:52,926,356-52,937,587
Genome
hg38
Position
chrX:52,897,330-52,908,560
HGNC
HGNC:31962 HGNC
Ensembl
ENSG00000179304 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Ranking
ClinVar
0
0
0
0
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
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 TMEM29B
HGNC HGNC:31962 HGNC
Ensembl ENSG00000179304 Ensembl
AllianceGenome HGNC:31962
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000593751.7 hg38 chrX 52,897,400 52,908,556 11,157
ENST00000509613.1 hg38 chrX 52,899,383 52,908,560 9,178
ENST00000416841.8 hg38 chrX 52,897,330 52,908,560 11,231
ENST00000616419.4 hg38 chrX 52,897,313 52,908,560 11,248
ENST00000616419.4 hg19 chrX 52,926,339 52,937,587 11,249
ENST00000416841.8 hg19 chrX 52,926,356 52,937,587 11,232
ENST00000593751.7 hg19 chrX 52,926,426 52,937,583 11,158
ENST00000509613.1 hg19 chrX 52,928,409 52,937,587 9,179
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