FAM234B family with sequence similarity 234 member B

Information
Symbol
FAM234B
Type
protein-coding
Description
family with sequence similarity 234 member B
Entrez Gene ID
57613
Genome
hg19
Position
chr12:13,197,315-13,236,383
Genome
hg38
Position
chr12:13,044,381-13,083,449
MIM
617838 OMIM
HGNC
HGNC:29288 HGNC
Ensembl
ENSG00000084444 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 14
Likely benign 0 16
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
88
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 :
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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 KIAA1467
MIM 617838 OMIM
HGNC HGNC:29288 HGNC
Ensembl ENSG00000084444 Ensembl
AllianceGenome HGNC:29288
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000197268.13 hg38 chr12 13,044,381 13,083,449 39,069
ENST00000197268.13 hg19 chr12 13,197,315 13,236,383 39,069
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