Variant #0000999054 (NC_000011.9:g.46895100C>T, NM_002334.3:c.4274G>A (LRP4))

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.46895100C>T
DNA change (hg38) -
Published as LRP4(NM_002334.3):c.4274G>A (p.(Arg1425Gln))
ISCN -
DB-ID LRP4_000077
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) 0.00015 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 2024-08-28 13:16:32 +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     
LRP4 NM_002334.3 ?/. - c.4274G>A r.(?) p.(Arg1425Gln)
LRP4-AS1 NR_038909.1 ?/. - n.673C>T r.(?) -


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