FAM110C family with sequence similarity 110 member C

Information
Symbol
FAM110C
Type
protein-coding
Description
family with sequence similarity 110 member C
Entrez Gene ID
642273
Genome
hg19
Position
chr2:38,814-46,505
Genome
hg38
Position
chr2:38,814-46,505
MIM
611395 OMIM
HGNC
HGNC:33340 HGNC
Ensembl
ENSG00000184731 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Uncertain significance 0 70
Ranking
ClinVar
0
0
0
70
4
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 :
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
MIM 611395 OMIM
HGNC HGNC:33340 HGNC
Ensembl ENSG00000184731 Ensembl
AllianceGenome HGNC:33340
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000327669.5 hg38 chr2 38,814 46,505 7,692
ENST00000327669.5 hg19 chr2 38,814 46,505 7,692
Genome browser