Variant #0001060435 (NC_000013.10:g.113459346A>G, NM_015205.2:c.238A>G (ATP11A))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.113459346A>G
DNA change (hg38) g.112805032A>G
Published as -
ISCN -
DB-ID ATP11A_000024
Variant remarks in vitro expression shows no effect on correct protein sorting and targeting
Reference PubMed: Sun 2020
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 2025-12-02 13:29:51 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP11A NM_015205.2 -?/. - c.238A>G - p.Ile80Val


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