FAM229B family with sequence similarity 229 member B

Information
Symbol
FAM229B
Type
protein-coding
Description
family with sequence similarity 229 member B
Entrez Gene ID
619208
Genome
hg19
Position
chr6:112,408,794-112,423,993
Genome
hg38
Position
chr6:112,087,591-112,102,790
HGNC
HGNC:33858 HGNC
Ensembl
ENSG00000203778 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
16
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
SYNONYM C6orf225
HGNC HGNC:33858 HGNC
Ensembl ENSG00000203778 Ensembl
AllianceGenome HGNC:33858
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000604268.1 hg38 chr6 112,087,638 112,100,895 13,258
ENST00000368656.7 hg38 chr6 112,087,591 112,102,790 15,200
ENST00000368656.7 hg19 chr6 112,408,794 112,423,993 15,200
ENST00000604268.1 hg19 chr6 112,408,841 112,422,098 13,258
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