Genomic variant #0000240490

Individual ID 00146687
Chromosome 19
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47248979C>G
DNA change (hg38) g.46745722C>G
Published as -
ISCN -
DB-ID FKRP_000033 See all 16 reported entries
Variant remarks -
Reference PubMed: Walter
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site BfaI-
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Rolf Stucka
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FKRP NM_024301.4 -/. 1 c.-621C>G r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000147543 DNA SEQ - - FKRP 3 Rolf Stucka