Genomic variant #0000240636

Individual ID 00146760
Chromosome 19
Allele Parent #2
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.47259848del
DNA change (hg38) g.46756591del
Published as 1136delG
ISCN -
DB-ID FKRP_000119 See all 2 reported entries
Variant remarks not in 320 control chromosomes
Reference PubMed: Guglieri 2007
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FKRP NM_024301.4 +/. 4 c.1141del r.(?) p.(Ala381Glnfs*47)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000147616 DNA SEQ - - FKRP 2 Johan den Dunnen