MUC16 mucin 16, cell surface associated

Information
Symbol
MUC16
Type
protein-coding
Description
mucin 16, cell surface associated
Entrez Gene ID
94025
Genome
hg19
Position
chr19:8,959,520-9,092,018
Genome
hg38
Position
chr19:8,848,844-8,981,342
MIM
606154 OMIM
HGNC
HGNC:15582 HGNC
Ensembl
ENSG00000181143 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 26
Benign 0 600
Likely benign 0 488
Uncertain significance 0 2
Ranking
ClinVar
0
0
110
944
36
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 :
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 CA125
MIM 606154 OMIM
HGNC HGNC:15582 HGNC
Ensembl ENSG00000181143 Ensembl
AllianceGenome HGNC:15582
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000397910.8 hg38 chr19 8,848,844 8,981,342 132,499
ENST00000710610.1 hg38 chr19 8,848,844 9,010,390 161,547
ENST00000710609.1 hg38 chr19 8,848,844 9,010,390 161,547
ENST00000711672.1 hg38 chr19 8,848,844 9,010,390 161,547
ENST00000397910.8 hg19 chr19 8,959,520 9,092,018 132,499
ENST00000711672.1 hg19 chr19 8,959,520 9,121,066 161,547
ENST00000710609.1 hg19 chr19 8,959,520 9,121,066 161,547
ENST00000710610.1 hg19 chr19 8,959,520 9,121,066 161,547
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