Variant #0000322728 (NC_000012.11:g.31244669A>G, NM_030653.3:c.1106A>G (DDX11))

Chromosome 12
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.31244669A>G
DNA change (hg38) g.31091735A>G
Published as DDX11(NM_001257144.1):c.1106A>G (p.(Tyr369Cys)), DDX11(NM_030653.4):c.1106A>G (p.Y369C)
ISCN -
DB-ID DDX11_000021 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) Retrieve
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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX11 NM_030653.3 ?/. - c.1106A>G r.(?) p.(Tyr369Cys)


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