FAM118A family with sequence similarity 118 member A

Information
Symbol
FAM118A
Type
protein-coding
Description
family with sequence similarity 118 member A
Entrez Gene ID
55007
Genome
hg19
Position
chr22:45,704,863-45,737,836
Genome
hg38
Position
chr22:45,308,982-45,341,955
HGNC
HGNC:1313 HGNC
Ensembl
ENSG00000100376 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 1 0
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
38
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 :
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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 C22orf8
HGNC HGNC:1313 HGNC
Ensembl ENSG00000100376 Ensembl
AllianceGenome HGNC:1313
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000405673.5 hg38 chr22 45,310,124 45,329,412 19,289
ENST00000216214.7 hg38 chr22 45,308,982 45,341,955 32,974
ENST00000441876.7 hg38 chr22 45,309,934 45,341,955 32,022
ENST00000216214.7 hg19 chr22 45,704,863 45,737,836 32,974
ENST00000441876.7 hg19 chr22 45,705,815 45,737,836 32,022
ENST00000405673.5 hg19 chr22 45,706,005 45,725,293 19,289
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