Variant #0000617715 (NC_000019.9:g.47249364_47249373dup, NC_000019.9(NM_024301.4):c.-253+17_-253+26dup (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.47249364_47249373dup
DNA change (hg38) g.46746107_46746116dup
Published as FKRP(NM_001039885.2):c.-305+4_-305+5insGGCCGGGCCG (p.(=))
ISCN -
DB-ID FKRP_000241
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRN4 NM_001039877.1 -?/. - c.282+45_282+54dup r.(=) p.(=)
FKRP NM_024301.4 -?/. - c.-253+17_-253+26dup r.(=) p.(=)


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