FAM227A family with sequence similarity 227 member A

Information
Symbol
FAM227A
Type
protein-coding
Description
family with sequence similarity 227 member A
Entrez Gene ID
646851
Genome
hg19
Position
chr22:38,974,123-39,052,397
Genome
hg38
Position
chr22:38,578,118-38,656,392
HGNC
HGNC:44197 HGNC
Ensembl
ENSG00000184949 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 70
Ranking
ClinVar
0
0
0
72
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 :
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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
HGNC HGNC:44197 HGNC
Ensembl ENSG00000184949 Ensembl
AllianceGenome HGNC:44197
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000540952.6 hg38 chr22 38,578,120 38,656,629 78,510
ENST00000355830.11 hg38 chr22 38,582,169 38,656,303 74,135
ENST00000535113.7 hg38 chr22 38,578,118 38,656,392 78,275
ENST00000535113.7 hg19 chr22 38,974,123 39,052,397 78,275
ENST00000540952.6 hg19 chr22 38,974,125 39,052,634 78,510
ENST00000355830.11 hg19 chr22 38,978,174 39,052,308 74,135
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