Variant #0000697179 (NC_000017.10:g.58234014G>A, NM_000717.3:c.206G>A (CA4))

Chromosome 17
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.58234014G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CA4_000014 See all 4 reported entries
Variant remarks expression cloning shows minimal effect on enzyme activity, defective protein processing, impaired trafficking to cell surface resulting in abnormal intracellular retention
Reference PubMed: Datta 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-10-07 14:07:28 +02:00 (CEST)
Date last edited 2020-10-07 14:09:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CA4 NM_000717.3 +/. - c.206G>A - p.Arg69His


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