FAM186B family with sequence similarity 186 member B

Information
Symbol
FAM186B
Type
protein-coding
Description
family with sequence similarity 186 member B
Entrez Gene ID
84070
Genome
hg19
Position
chr12:49,981,288-49,999,422
Genome
hg38
Position
chr12:49,587,505-49,605,639
HGNC
HGNC:25296 HGNC
Ensembl
ENSG00000135436 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 48
Likely benign 0 48
Uncertain significance 0 132
Ranking
ClinVar
0
0
20
206
2
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 C12orf25
HGNC HGNC:25296 HGNC
Ensembl ENSG00000135436 Ensembl
AllianceGenome HGNC:25296
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000257894.2 hg38 chr12 49,587,505 49,605,639 18,135
ENST00000551047.5 hg38 chr12 49,583,208 49,605,618 22,411
ENST00000551047.5 hg19 chr12 49,976,991 49,999,401 22,411
ENST00000257894.2 hg19 chr12 49,981,288 49,999,422 18,135
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