FAM186A family with sequence similarity 186 member A

Information
Symbol
FAM186A
Type
protein-coding
Description
family with sequence similarity 186 member A
Entrez Gene ID
121006
Genome
hg19
Position
chr12:50,721,092-50,790,392
Genome
hg38
Position
chr12:50,327,309-50,396,609
HGNC
HGNC:26980 HGNC
Ensembl
ENSG00000185958 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 72
Uncertain significance 0 236
Ranking
ClinVar
0
0
2
312
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:26980 HGNC
Ensembl ENSG00000185958 Ensembl
AllianceGenome HGNC:26980
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000543111.5 hg38 chr12 50,326,230 50,396,622 70,393
ENST00000327337.6 hg38 chr12 50,327,309 50,396,609 69,301
ENST00000543096.5 hg38 chr12 50,326,230 50,350,885 24,656
ENST00000543096.5 hg19 chr12 50,720,013 50,744,668 24,656
ENST00000543111.5 hg19 chr12 50,720,013 50,790,405 70,393
ENST00000327337.6 hg19 chr12 50,721,092 50,790,392 69,301
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