Variant #0000617717 (NC_000019.9:g.47249369_47249373del, NC_000019.9(NM_024301.4):c.-253+22_-253+26del (FKRP))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47249369_47249373del
DNA change (hg38) g.46746112_46746116del
Published as -
ISCN -
DB-ID FKRP_000242
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRN4 NM_001039877.1 -?/. - c.282+50_282+54del r.(=) p.(=)
FKRP NM_024301.4 -?/. - c.-253+22_-253+26del r.(=) p.(=)


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