FAM98C family with sequence similarity 98 member C

Information
Symbol
FAM98C
Type
protein-coding
Description
family with sequence similarity 98 member C
Entrez Gene ID
147965
Genome
hg19
Position
chr19:38,893,733-38,899,724
Genome
hg38
Position
chr19:38,403,093-38,409,084
HGNC
HGNC:27119 HGNC
Ensembl
ENSG00000130244 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 10
Likely benign 0 22
Uncertain significance 0 34
Ranking
ClinVar
0
0
2
62
2
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 :
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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:27119 HGNC
Ensembl ENSG00000130244 Ensembl
AllianceGenome HGNC:27119
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000343358.11 hg38 chr19 38,403,154 38,409,084 5,931
ENST00000588262.5 hg38 chr19 38,403,135 38,409,040 5,906
ENST00000252530.10 hg38 chr19 38,403,093 38,409,084 5,992
ENST00000252530.10 hg19 chr19 38,893,733 38,899,724 5,992
ENST00000588262.5 hg19 chr19 38,893,775 38,899,680 5,906
ENST00000343358.11 hg19 chr19 38,893,794 38,899,724 5,931
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