Variant #0000282320 (NC_000011.9:g.46890165C>T, NM_002334.3:c.4937G>A (LRP4))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46890165C>T
DNA change (hg38) g.46868614C>T
Published as LRP4(NM_002334.4):c.4937G>A (p.R1646Q), LRP4-AS1(NR_038909.1):n.198-4460C>T
ISCN -
DB-ID LRP4_000021
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) 0.68041 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRP4 NM_002334.3 -/. - c.4937G>A r.(?) p.(Arg1646Gln)
LRP4-AS1 NR_038909.1 -/. - n.198-4460C>T r.(?) -


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