FAM50B family with sequence similarity 50 member B

Information
Symbol
FAM50B
Type
protein-coding
Description
family with sequence similarity 50 member B
Entrez Gene ID
26240
Genome
hg19
Position
chr6:3,849,620-3,851,554
Genome
hg38
Position
chr6:3,849,386-3,851,320
MIM
614686 OMIM
HGNC
HGNC:18789 HGNC
Ensembl
ENSG00000145945 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
36
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 D6S2654E
SYNONYM X5L
MIM 614686 OMIM
HGNC HGNC:18789 HGNC
Ensembl ENSG00000145945 Ensembl
AllianceGenome HGNC:18789
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000380274.2 hg38 chr6 3,849,386 3,851,320 1,935
ENST00000648326.1 hg38 chr6 3,849,373 3,851,317 1,945
ENST00000648326.1 hg19 chr6 3,849,607 3,851,551 1,945
ENST00000380274.2 hg19 chr6 3,849,620 3,851,554 1,935
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