Variant #0000435675 (NC_000010.10:g.92679964C>G, NM_014391.2:c.169G>C (ANKRD1))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.92679964C>G
DNA change (hg38) g.90920207C>G
Published as -
ISCN -
DB-ID ANKRD1_000007 See all 2 reported entries
Variant remarks expression cloning normal cellular localization, significantly reduced repressor activity
Reference PubMed: Duboscq-Bidot 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-04-17 10:20:00 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD1 NM_014391.2 +/. 2 c.169G>C r.(?) p.Glu57Gln


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