FAM117A family with sequence similarity 117 member A

Information
Symbol
FAM117A
Type
protein-coding
Description
family with sequence similarity 117 member A
Entrez Gene ID
81558
Genome
hg19
Position
chr17:47,787,694-47,841,493
Genome
hg38
Position
chr17:49,710,332-49,764,131
HGNC
HGNC:24179 HGNC
Ensembl
ENSG00000121104 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
48
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:24179 HGNC
Ensembl ENSG00000121104 Ensembl
AllianceGenome HGNC:24179
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000240364.7 hg38 chr17 49,710,332 49,764,131 53,800
ENST00000513602.5 hg38 chr17 49,710,995 49,788,592 77,598
ENST00000240364.7 hg19 chr17 47,787,694 47,841,493 53,800
ENST00000513602.5 hg19 chr17 47,788,357 47,865,954 77,598
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