FAM98A family with sequence similarity 98 member A

Information
Symbol
FAM98A
Type
protein-coding
Description
family with sequence similarity 98 member A
Entrez Gene ID
25940
Genome
hg19
Position
chr2:33,808,727-33,824,366
Genome
hg38
Position
chr2:33,583,660-33,599,299
HGNC
HGNC:24520 HGNC
Ensembl
ENSG00000119812 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
60
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:24520 HGNC
Ensembl ENSG00000119812 Ensembl
AllianceGenome HGNC:24520
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000690423.1 hg38 chr2 33,583,062 33,599,249 16,188
ENST00000403368.1 hg38 chr2 33,583,670 33,599,291 15,622
ENST00000238823.13 hg38 chr2 33,583,660 33,599,299 15,640
ENST00000689713.1 hg38 chr2 33,583,686 33,599,347 15,662
ENST00000690423.1 hg19 chr2 33,808,129 33,824,316 16,188
ENST00000238823.13 hg19 chr2 33,808,727 33,824,366 15,640
ENST00000403368.1 hg19 chr2 33,808,737 33,824,358 15,622
ENST00000689713.1 hg19 chr2 33,808,753 33,824,414 15,662
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