FAM136A family with sequence similarity 136 member A

Information
Symbol
FAM136A
Type
protein-coding
Description
family with sequence similarity 136 member A
Entrez Gene ID
84908
Genome
hg19
Position
chr2:70,523,108-70,529,199
Genome
hg38
Position
chr2:70,295,976-70,302,067
MIM
616275 OMIM
HGNC
HGNC:25911 HGNC
Ensembl
ENSG00000035141 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 18
Likely benign 0 14
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 16
Ranking
ClinVar
0
0
2
46
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
MIM 616275 OMIM
HGNC HGNC:25911 HGNC
Ensembl ENSG00000035141 Ensembl
AllianceGenome HGNC:25911
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000037869.8 hg38 chr2 70,295,976 70,302,067 6,092
ENST00000430566.6 hg38 chr2 70,295,976 70,302,067 6,092
ENST00000037869.8 hg19 chr2 70,523,108 70,529,199 6,092
ENST00000430566.6 hg19 chr2 70,523,108 70,529,199 6,092
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