MYOCD myocardin

Information
Symbol
MYOCD
Type
protein-coding
Description
myocardin
Entrez Gene ID
93649
Genome
hg19
Position
chr17:12,569,207-12,672,266
Genome
hg38
Position
chr17:12,665,890-12,768,949
MIM
606127 OMIM
HGNC
HGNC:16067 HGNC
Ensembl
ENSG00000141052 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 4
Benign 0 72
Likely benign 0 6
Conflicting classifications of pathogenicity 0 2
no classification for the single variant 0 4
Uncertain significance 0 98
Ranking
ClinVar
0
0
8
164
8
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 MGBL
SYNONYM MYCD
MIM 606127 OMIM
HGNC HGNC:16067 HGNC
Ensembl ENSG00000141052 Ensembl
AllianceGenome HGNC:16067
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000425538.6 hg38 chr17 12,665,890 12,768,949 103,060
ENST00000343344.8 hg38 chr17 12,666,189 12,763,644 97,456
ENST00000425538.6 hg19 chr17 12,569,207 12,672,266 103,060
ENST00000343344.8 hg19 chr17 12,569,506 12,666,961 97,456
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