FAM237B family with sequence similarity 237 member B

Information
Symbol
FAM237B
Type
protein-coding
Description
family with sequence similarity 237 member B
Entrez Gene ID
107986818
Genome
hg19
Position
chr7:89,945,817-89,950,618
Genome
hg38
Position
chr7:90,316,503-90,321,304
HGNC
HGNC:53217 HGNC
Ensembl
ENSG00000283267 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
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
[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:53217 HGNC
Ensembl ENSG00000283267 Ensembl
AllianceGenome HGNC:53217
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000637645.2 hg38 chr7 90,316,503 90,321,304 4,802
ENST00000692316.1 hg38 chr7 90,316,807 90,321,304 4,498
ENST00000637645.2 hg19 chr7 89,945,817 89,950,618 4,802
ENST00000692316.1 hg19 chr7 89,946,121 89,950,618 4,498
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