FAM133A family with sequence similarity 133 member A

Information
Symbol
FAM133A
Type
protein-coding
Description
family with sequence similarity 133 member A
Entrez Gene ID
286499
Genome
hg19
Position
chrX:92,929,205-92,967,264
Genome
hg38
Position
chrX:93,674,206-93,712,265
HGNC
HGNC:26748 HGNC
Ensembl
ENSG00000179083 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 6 0
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
18
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
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 CT115
HGNC HGNC:26748 HGNC
Ensembl ENSG00000179083 Ensembl
AllianceGenome HGNC:26748
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000683942.1 hg38 chrX 93,674,206 93,712,265 38,060
ENST00000322139.4 hg38 chrX 93,674,013 93,712,274 38,262
ENST00000332647.5 hg38 chrX 93,674,206 93,712,265 38,060
ENST00000322139.4 hg19 chrX 92,929,012 92,967,273 38,262
ENST00000332647.5 hg19 chrX 92,929,205 92,967,264 38,060
ENST00000683942.1 hg19 chrX 92,929,205 92,967,264 38,060
Genome browser