FAM222A family with sequence similarity 222 member A

Information
Symbol
FAM222A
Type
protein-coding
Description
family with sequence similarity 222 member A
Entrez Gene ID
84915
Genome
hg19
Position
chr12:110,151,630-110,208,300
Genome
hg38
Position
chr12:109,713,825-109,770,495
HGNC
HGNC:25915 HGNC
Ensembl
ENSG00000139438 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 8
Likely benign 0 4
Uncertain significance 0 76
Ranking
ClinVar
0
0
0
90
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 :
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 C12orf34
HGNC HGNC:25915 HGNC
Ensembl ENSG00000139438 Ensembl
AllianceGenome HGNC:25915
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000358906.3 hg38 chr12 109,734,767 109,770,494 35,728
ENST00000538780.2 hg38 chr12 109,713,825 109,770,495 56,671
ENST00000538780.2 hg19 chr12 110,151,630 110,208,300 56,671
ENST00000358906.3 hg19 chr12 110,172,572 110,208,299 35,728
Genome browser