FAM236C family with sequence similarity 236 member C

Information
Symbol
FAM236C
Type
protein-coding
Description
family with sequence similarity 236 member C
Entrez Gene ID
109729126
Genome
hg19
Position
chrX:72,132,453-72,133,238
Genome
hg38
Position
chrX:72,912,615-72,913,401
HGNC
HGNC:52641 HGNC
Ensembl
ENSG00000283594 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Ranking
ClinVar
0
0
0
0
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
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
SYNONYM FAM236D
HGNC HGNC:52641 HGNC
Ensembl ENSG00000283594 Ensembl
AllianceGenome HGNC:52641
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000636532.1 hg38 chrX 72,912,615 72,913,401 787
ENST00000636267.1 hg38 chrX 72,912,615 72,913,401 787
ENST00000636532.1 hg19 chrX 72,132,453 72,133,238 786
ENST00000636267.1 hg19 chrX 72,132,453 72,133,238 786
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