FAM120C family with sequence similarity 120 member C

Information
Symbol
FAM120C
Type
protein-coding
Description
family with sequence similarity 120 member C
Entrez Gene ID
54954
Genome
hg19
Position
chrX:54,094,757-54,209,687
Genome
hg38
Position
chrX:54,068,324-54,183,254
MIM
300741 OMIM
HGNC
HGNC:16949 HGNC
Ensembl
ENSG00000184083 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 10
not provided 6 0
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
64
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
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 CXorf17
SYNONYM ORF34
MIM 300741 OMIM
HGNC HGNC:16949 HGNC
Ensembl ENSG00000184083 Ensembl
AllianceGenome HGNC:16949
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000328235.4 hg38 chrX 54,072,253 54,183,255 111,003
ENST00000375180.7 hg38 chrX 54,068,324 54,183,254 114,931
ENST00000477084.1 hg38 chrX 54,173,789 54,183,281 9,493
ENST00000375180.7 hg19 chrX 54,094,757 54,209,687 114,931
ENST00000328235.4 hg19 chrX 54,098,686 54,209,688 111,003
ENST00000477084.1 hg19 chrX 54,200,222 54,209,714 9,493
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