FAM230H family with sequence similarity 230 member H

Information
Symbol
FAM230H
Type
ncRNA
Description
family with sequence similarity 230 member H
Entrez Gene ID
100996335
Genome
hg19
Position
chr22:21,655,280-21,664,170
Genome
hg38
Position
chr22:21,300,991-21,309,881
HGNC
HGNC:53977 HGNC
Ensembl
ENSG00000206142 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 4 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:53977 HGNC
Ensembl ENSG00000206142 Ensembl
AllianceGenome HGNC:53977
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000436681.5 hg38 chr22 21,300,991 21,309,881 8,891
ENST00000416615.5 hg38 chr22 21,300,997 21,325,042 24,046
ENST00000452952.1 hg38 chr22 21,321,948 21,324,967 3,020
ENST00000447720.5 hg38 chr22 21,300,990 21,325,042 24,053
ENST00000447720.5 hg19 chr22 21,655,279 21,679,331 24,053
ENST00000436681.5 hg19 chr22 21,655,280 21,664,170 8,891
ENST00000416615.5 hg19 chr22 21,655,286 21,679,331 24,046
ENST00000452952.1 hg19 chr22 21,676,237 21,679,256 3,020
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