Genomic variant #0000235503

Individual ID 00143818
Chromosome 9
Allele Paternal (inferred)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.?
DNA change (hg38) -
Published as -
ISCN -
DB-ID MUSK_000013
Variant remarks deletion detected on RNA
Reference PubMed: Gallenmuler 2014, Journal: Gallenmuler 2014
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Genomic location of variant could not be determined
Owner Johan den Dunnen




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
MUSK NM_005592.3 +/. 1i_3i c.(79+1_80-1)_(358+1_359-1)del - r.80_358del p.Ala27_Lys120delinsGlu



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000144677 DNA;RNA RT-PCR;SEQ - - MUSK 2 Johan den Dunnen