Variant #0000282327 (NC_000002.11:g.44190789T>C, NM_133259.3:c.1426A>G (LRPPRC))

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.44190789T>C
DNA change (hg38) g.43963650T>C
Published as LRPPRC(NM_133259.3):c.1426A>G (p.T476A), LRPPRC(NM_133259.4):c.1426A>G (p.T476A)
ISCN -
DB-ID LRPPRC_000024 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) 0.00095 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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRPPRC NM_133259.3 ?/. - c.1426A>G r.(?) p.(Thr476Ala)


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