FAM216A family with sequence similarity 216 member A

Information
Symbol
FAM216A
Type
protein-coding
Description
family with sequence similarity 216 member A
Entrez Gene ID
29902
Genome
hg19
Position
chr12:110,906,650-110,928,190
Genome
hg38
Position
chr12:110,468,845-110,490,385
HGNC
HGNC:30180 HGNC
Ensembl
ENSG00000204856 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
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
[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 C12orf24
SYNONYM HSU79274
HGNC HGNC:30180 HGNC
Ensembl ENSG00000204856 Ensembl
AllianceGenome HGNC:30180
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000377673.10 hg38 chr12 110,468,845 110,490,385 21,541
ENST00000377673.10 hg19 chr12 110,906,650 110,928,190 21,541
Genome browser