Variant #0000322721 (NC_000012.11:g.31236856A>G, NM_030653.3:c.254A>G (DDX11))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31236856A>G
DNA change (hg38) g.31083922A>G
Published as DDX11(NM_001257144.1):c.254A>G (p.(His85Arg)), DDX11(NM_030653.3):c.254A>G (p.H85R)
ISCN -
DB-ID DDX11_000008 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) 0.00543 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX11 NM_030653.3 -?/. - c.254A>G r.(?) p.(His85Arg)


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