FAM236B family with sequence similarity 236 member B

Information
Symbol
FAM236B
Type
protein-coding
Description
family with sequence similarity 236 member B
Entrez Gene ID
100132304
Genome
hg19
Position
chrX:72,001,689-72,002,484
Genome
hg38
Position
chrX:72,781,865-72,782,660
HGNC
HGNC:52640 HGNC
Ensembl
ENSG00000268994 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
HGNC HGNC:52640 HGNC
Ensembl ENSG00000268994 Ensembl
AllianceGenome HGNC:52640
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000596535.3 hg38 chrX 72,781,865 72,782,660 796
ENST00000596535.3 hg19 chrX 72,001,689 72,002,484 796
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