Variant #0000926915 (NC_000019.9:g.47260071C>A, NM_024301.4:c.1364C>A (FKRP))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47260071C>A
DNA change (hg38) -
Published as FKRP(NM_024301.5):c.1364C>A (p.A455D)
ISCN -
DB-ID FKRP_000054 See all 18 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
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.-10384G>T r.(?) p.(=)
SLC1A5 NM_001145144.1 +/. - c.*18696G>T r.(=) p.(=)
FKRP NM_024301.4 +/. - c.1364C>A r.(?) p.(Ala455Asp)


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