FAM171A2 family with sequence similarity 171 member A2

Information
Symbol
FAM171A2
Type
protein-coding
Description
family with sequence similarity 171 member A2
Entrez Gene ID
284069
Genome
hg19
Position
chr17:42,430,583-42,441,221
Genome
hg38
Position
chr17:44,353,215-44,363,853
HGNC
HGNC:30480 HGNC
Ensembl
ENSG00000161682 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 86
Ranking
ClinVar
0
0
0
86
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 :
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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:30480 HGNC
Ensembl ENSG00000161682 Ensembl
AllianceGenome HGNC:30480
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000293443.12 hg38 chr17 44,353,215 44,363,853 10,639
ENST00000293443.12 hg19 chr17 42,430,583 42,441,221 10,639
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