Variant #0001084499 (NC_000019.9:g.47258710G>C, NM_024301.4:c.3G>C (FKRP))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.47258710G>C
DNA change (hg38) g.46755453G>C
Published as -
ISCN -
DB-ID chr19_008860
Variant remarks SMuRF classification damaging_severe (fitness normalized score -2,919062986)
Reference PubMed: Ma 2024, PubMed: Ma 2024
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2026-09-06 12:03:18 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FKRP NM_024301.4 +/. - c.3G>C - p.Met1?


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