Variant #0000268660 (NC_000011.9:g.47256343G>A, NM_000107.2:c.738G>A (DDB2))

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.47256343G>A
DNA change (hg38) g.47234792G>A
Published as DDB2(NM_000107.2):c.738G>A (p.T246=)
ISCN -
DB-ID DDB2_000003 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) 0.00292 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-30 13:35:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDB2 NM_000107.2 -/. - c.738G>A r.(?) p.(Thr246=)
ACP2 NM_001610.2 -/. - c.*5324C>T r.(=) p.(=)


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