FAM98B family with sequence similarity 98 member B

Information
Symbol
FAM98B
Type
protein-coding
Description
family with sequence similarity 98 member B
Entrez Gene ID
283742
Genome
hg19
Position
chr15:38,746,328-38,779,911
Genome
hg38
Position
chr15:38,454,127-38,487,710
MIM
616142 OMIM
HGNC
HGNC:26773 HGNC
Ensembl
ENSG00000171262 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 46
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
MIM 616142 OMIM
HGNC HGNC:26773 HGNC
Ensembl ENSG00000171262 Ensembl
AllianceGenome HGNC:26773
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000491535.5 hg38 chr15 38,454,154 38,483,665 29,512
ENST00000397609.6 hg38 chr15 38,454,127 38,487,710 33,584
ENST00000397609.6 hg19 chr15 38,746,328 38,779,911 33,584
ENST00000491535.5 hg19 chr15 38,746,355 38,775,866 29,512
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