FAM185A family with sequence similarity 185 member A

Information
Symbol
FAM185A
Type
protein-coding
Description
family with sequence similarity 185 member A
Entrez Gene ID
222234
Genome
hg19
Position
chr7:102,389,446-102,449,672
Genome
hg38
Position
chr7:102,748,999-102,809,225
HGNC
HGNC:22412 HGNC
Ensembl
ENSG00000222011 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 36
Ranking
ClinVar
0
0
0
38
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 :
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:22412 HGNC
Ensembl ENSG00000222011 Ensembl
AllianceGenome HGNC:22412
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409231.7 hg38 chr7 102,749,028 102,808,840 59,813
ENST00000413034.3 hg38 chr7 102,748,999 102,809,225 60,227
ENST00000413034.3 hg19 chr7 102,389,446 102,449,672 60,227
ENST00000409231.7 hg19 chr7 102,389,475 102,449,287 59,813
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