Variant #0000606343 (NC_000002.11:g.170112698G>C, NM_004525.2:c.2688C>G (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.170112698G>C
DNA change (hg38) g.169256188G>C
Published as LRP2(NM_004525.2):c.2688C>G (p.(His896Gln)), LRP2(NM_004525.3):c.2688C>G (p.H896Q)
ISCN -
DB-ID LRP2_000089 See all 3 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 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRP2 NM_004525.2 ?/. - c.2688C>G r.(?) p.(His896Gln)


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