Variant #0000510214 (NC_000002.11:g.170151226G>T, NC_000002.11(NM_004525.2):c.428-6C>A (LRP2))

Chromosome 2
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.170151226G>T
DNA change (hg38) g.169294716G>T
Published as LRP2(NM_004525.2):c.428-6C>A (p.(=)), LRP2(NM_004525.3):c.428-6C>A
ISCN -
DB-ID LRP2_000216 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 14:54:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRP2 NM_004525.2 ?/. - c.428-6C>A r.(=) p.(=)


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