Variant #0000691071 (NC_000011.9:g.46889546C>T, NM_002334.3:c.5071G>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.46889546C>T
DNA change (hg38) -
Published as LRP4(NM_002334.3):c.5071G>A (p.E1691K, p.(Glu1691Lys))
ISCN -
DB-ID LRP4_000044 See all 2 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) 0.00037 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRP4 NM_002334.3 ?/. - c.5071G>A r.(?) p.(Glu1691Lys)
LRP4-AS1 NR_038909.1 ?/. - n.198-5079C>T r.(?) -


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