Variant #0000979806 (NC_000011.9:g.68080234_68080242dup, NM_002335.4:c.52_60dup (LRP5))

Chromosome 11
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.68080234_68080242dup
DNA change (hg38) -
Published as LRP5(NM_002335.4):c.52_60dup (p.(Leu18_Leu20dup))
ISCN -
DB-ID LRP5_000482
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 2024-04-19 20:27:30 +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     
LRP5 NM_002335.4 ?/. - c.52_60dup r.(?) p.(Leu18_Leu20dup)


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