Variant #0001056726 (NC_000019.9:g.47260125T>G, NM_024301.4:c.1418T>G (FKRP))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.47260125T>G
DNA change (hg38) -
Published as FKRP(NM_024301.5):c.1418T>G (p.(Phe473Cys))
ISCN -
DB-ID FKRP_000331
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRN4 NM_001039877.1 ?/. - c.-10438A>C r.(?) p.(=)
SLC1A5 NM_001145144.1 ?/. - c.*18642A>C r.(=) p.(=)
FKRP NM_024301.4 ?/. - c.1418T>G r.(?) p.(Phe473Cys)


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