FAM230B family with sequence similarity 230 member B

Information
Symbol
FAM230B
Type
ncRNA
Description
family with sequence similarity 230 member B
Entrez Gene ID
642633
Genome
hg19
Position
chr22:21,522,047-21,546,445
Genome
hg38
Position
chr22:21,167,758-21,192,156
HGNC
HGNC:32943 HGNC
Ensembl
ENSG00000215498 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 10 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:32943 HGNC
Ensembl ENSG00000215498 Ensembl
AllianceGenome HGNC:32943
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000415376.5 hg38 chr22 21,167,829 21,192,149 24,321
ENST00000424410.1 hg38 chr22 21,169,946 21,182,974 13,029
ENST00000415704.5 hg38 chr22 21,167,853 21,173,530 5,678
ENST00000451257.5 hg38 chr22 21,167,758 21,192,156 24,399
ENST00000421576.5 hg38 chr22 21,167,885 21,183,322 15,438
ENST00000451257.5 hg19 chr22 21,522,047 21,546,445 24,399
ENST00000415376.5 hg19 chr22 21,522,118 21,546,438 24,321
ENST00000415704.5 hg19 chr22 21,522,142 21,527,819 5,678
ENST00000421576.5 hg19 chr22 21,522,174 21,537,611 15,438
ENST00000424410.1 hg19 chr22 21,524,235 21,537,263 13,029
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