FAM110A family with sequence similarity 110 member A

Information
Symbol
FAM110A
Type
protein-coding
Description
family with sequence similarity 110 member A
Entrez Gene ID
83541
Genome
hg19
Position
chr20:814,420-826,922
Genome
hg38
Position
chr20:833,777-846,279
MIM
611393 OMIM
HGNC
HGNC:16188 HGNC
Ensembl
ENSG00000125898 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
Uncertain significance 0 42
Ranking
ClinVar
0
0
0
46
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
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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 :
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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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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 C20orf55
SYNONYM F10
SYNONYM bA371L19.3
MIM 611393 OMIM
HGNC HGNC:16188 HGNC
Ensembl ENSG00000125898 Ensembl
AllianceGenome HGNC:16188
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000304189.6 hg38 chr20 833,777 846,279 12,503
ENST00000246100.3 hg38 chr20 836,068 846,279 10,212
ENST00000381939.1 hg38 chr20 833,784 846,279 12,496
ENST00000541082.2 hg38 chr20 841,275 846,279 5,005
ENST00000381941.8 hg38 chr20 833,715 846,277 12,563
ENST00000381941.8 hg19 chr20 814,358 826,920 12,563
ENST00000304189.6 hg19 chr20 814,420 826,922 12,503
ENST00000381939.1 hg19 chr20 814,427 826,922 12,496
ENST00000246100.3 hg19 chr20 816,711 826,922 10,212
ENST00000541082.2 hg19 chr20 821,918 826,922 5,005
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