Variant #0000727456 (NC_000019.9:g.47258844del, NM_024301.4:c.137del (FKRP))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47258844del
DNA change (hg38) -
Published as FKRP(NM_001039885.3):c.137delG (p.G46Afs*22)
ISCN -
DB-ID FKRP_000232
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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.-9156del r.(?) p.(=)
SLC1A5 NM_001145144.1 +?/. - c.*19924del r.(?) p.(=)
FKRP NM_024301.4 +?/. - c.137del r.(?) p.(Gly46AlafsTer22)


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