LSM12 LSM12 homolog

Information
Symbol
LSM12
Type
protein-coding
Description
LSM12 homolog
Entrez Gene ID
124801
Genome
hg19
Position
chr17:42,113,511-42,144,027
Genome
hg38
Position
chr17:44,036,143-44,066,659
MIM
611793 OMIM
HGNC
HGNC:26407 HGNC
Ensembl
ENSG00000161654 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 4
Ranking
ClinVar
0
0
0
4
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 :
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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 PNAS-135
MIM 611793 OMIM
HGNC HGNC:26407 HGNC
Ensembl ENSG00000161654 Ensembl
AllianceGenome HGNC:26407
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000293406.8 hg38 chr17 44,034,328 44,066,671 32,344
ENST00000591247.6 hg38 chr17 44,034,328 44,067,619 33,292
ENST00000585388.2 hg38 chr17 44,036,143 44,066,659 30,517
ENST00000293406.8 hg19 chr17 42,111,696 42,144,039 32,344
ENST00000591247.6 hg19 chr17 42,111,696 42,144,987 33,292
ENST00000585388.2 hg19 chr17 42,113,511 42,144,027 30,517
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