LSM14B LSM family member 14B

Information
Symbol
LSM14B
Type
protein-coding
Description
LSM family member 14B
Entrez Gene ID
149986
Genome
hg19
Position
chr20:60,697,531-60,710,430
Genome
hg38
Position
chr20:62,122,475-62,135,374
MIM
620689 OMIM
HGNC
HGNC:15887 HGNC
Ensembl
ENSG00000149657 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
48
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
SYNONYM C20orf40
SYNONYM FAM61B
SYNONYM FT005
SYNONYM LSM13
SYNONYM RAP55B
SYNONYM bA11M20.3
MIM 620689 OMIM
HGNC HGNC:15887 HGNC
Ensembl ENSG00000149657 Ensembl
AllianceGenome HGNC:15887
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000279068.11 hg38 chr20 62,122,475 62,135,374 12,900
ENST00000370915.5 hg38 chr20 62,122,461 62,128,030 5,570
ENST00000370915.5 hg19 chr20 60,697,517 60,703,086 5,570
ENST00000279068.11 hg19 chr20 60,697,531 60,710,430 12,900
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