MYF6 myogenic factor 6

Information
Symbol
MYF6
Type
protein-coding
Description
myogenic factor 6
Entrez Gene ID
4618
Genome
hg19
Position
chr12:81,101,413-81,103,253
Genome
hg38
Position
chr12:80,707,634-80,709,474
MIM
159991 OMIM
HGNC
HGNC:7566 HGNC
Ensembl
ENSG00000111046 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 6 16
Likely benign 0 24
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 74
Ranking
ClinVar
0
0
20
90
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 CNM3
SYNONYM MRF4
SYNONYM bHLHc4
SYNONYM myf-6
MIM 159991 OMIM
HGNC HGNC:7566 HGNC
Ensembl ENSG00000111046 Ensembl
AllianceGenome HGNC:7566
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000228641.4 hg38 chr12 80,707,634 80,709,474 1,841
ENST00000228641.4 hg19 chr12 81,101,413 81,103,253 1,841
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