Variant #0000544039 (NC_000011.9:g.47256961A>G, NM_000107.2:c.1021A>G (DDB2))

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.47256961A>G
DNA change (hg38) g.47235410A>G
Published as DDB2(NM_000107.2):c.1021A>G (p.K341E)
ISCN -
DB-ID DDB2_000018
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-08-31 14:25:22 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDB2 NM_000107.2 ?/. - c.1021A>G r.(?) p.(Lys341Glu)
ACP2 NM_001610.2 ?/. - c.*4706T>C r.(=) p.(=)


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