FAM217A family with sequence similarity 217 member A

Information
Symbol
FAM217A
Type
protein-coding
Description
family with sequence similarity 217 member A
Entrez Gene ID
222826
Genome
hg19
Position
chr6:4,068,601-4,079,371
Genome
hg38
Position
chr6:4,068,367-4,079,137
HGNC
HGNC:21362 HGNC
Ensembl
ENSG00000145975 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 18
Uncertain significance 0 72
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 :
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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 C6orf146
HGNC HGNC:21362 HGNC
Ensembl ENSG00000145975 Ensembl
AllianceGenome HGNC:21362
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000274673.8 hg38 chr6 4,068,367 4,079,137 10,771
ENST00000639338.1 hg38 chr6 4,068,696 4,087,027 18,332
ENST00000274673.8 hg19 chr6 4,068,601 4,079,371 10,771
ENST00000639338.1 hg19 chr6 4,068,930 4,087,261 18,332
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