FAM228A family with sequence similarity 228 member A

Information
Symbol
FAM228A
Type
protein-coding
Description
family with sequence similarity 228 member A
Entrez Gene ID
653140
Genome
hg19
Position
chr2:24,397,922-24,414,567
Genome
hg38
Position
chr2:24,175,053-24,191,698
HGNC
HGNC:34418 HGNC
Ensembl
ENSG00000186453 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 2 0
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
26
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 C2orf84
HGNC HGNC:34418 HGNC
Ensembl ENSG00000186453 Ensembl
AllianceGenome HGNC:34418
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000432434.2 hg38 chr2 24,175,288 24,200,846 25,559
ENST00000295150.8 hg38 chr2 24,175,053 24,191,698 16,646
ENST00000295150.8 hg19 chr2 24,397,922 24,414,567 16,646
ENST00000432434.2 hg19 chr2 24,398,157 24,423,715 25,559
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