SAMD4B sterile alpha motif domain containing 4B

Information
Symbol
SAMD4B
Type
protein-coding
Description
sterile alpha motif domain containing 4B
Entrez Gene ID
55095
Genome
hg19
Position
chr19:39,833,061-39,876,340
Genome
hg38
Position
chr19:39,342,421-39,385,700
MIM
619231 OMIM
HGNC
HGNC:25492 HGNC
Ensembl
ENSG00000179134 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 70
Ranking
ClinVar
0
0
0
70
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 :
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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 SMGB
SYNONYM Smaug2
MIM 619231 OMIM
HGNC HGNC:25492 HGNC
Ensembl ENSG00000179134 Ensembl
AllianceGenome HGNC:25492
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000598913.5 hg38 chr19 39,342,442 39,384,188 41,747
ENST00000596368.1 hg38 chr19 39,356,816 39,385,710 28,895
ENST00000314471.10 hg38 chr19 39,342,468 39,384,926 42,459
ENST00000610417.5 hg38 chr19 39,342,421 39,385,700 43,280
ENST00000610417.5 hg19 chr19 39,833,061 39,876,340 43,280
ENST00000598913.5 hg19 chr19 39,833,082 39,874,828 41,747
ENST00000314471.10 hg19 chr19 39,833,108 39,875,566 42,459
ENST00000596368.1 hg19 chr19 39,847,456 39,876,350 28,895
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