FAM86C1P family with sequence similarity 86 member C1, pseudogene

Information
Symbol
FAM86C1P
Type
unknown
Description
family with sequence similarity 86 member C1, pseudogene
Entrez Gene ID
55199
Genome
hg19
Position
chr11:71,498,583-71,510,706
Genome
hg38
Position
chr11:71,787,537-71,799,660
MIM
616124 OMIM
HGNC
HGNC:25561 HGNC
Ensembl
ENSG00000158483 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
SYNONYM FAM86C
SYNONYM FAM86C1
MIM 616124 OMIM
HGNC HGNC:25561 HGNC
Ensembl ENSG00000158483 Ensembl
AllianceGenome HGNC:25561
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000675931.1 hg38 chr11 71,787,537 71,799,660 12,124
ENST00000675931.1 hg19 chr11 71,498,583 71,510,706 12,124
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