Variant #0001060436 (NC_000013.10:g.113479770_113479771delinsTC, NM_015205.2:c.899_900delinsTC (ATP11A))

Chromosome 13
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.113479770_113479771delinsTC
DNA change (hg38) g.112825456_112825457delinsTC
Published as -
ISCN -
DB-ID ATP11A_000025
Variant remarks in vitro expression shows reduced ATP11A expression, incorrect subcellular protein localisation and reduced PS internalization in plasma membrane
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 13:36:15 +01:00 (CET)
Date last edited 2025-12-02 13:40:57 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP11A NM_015205.2 +/. - c.899_900delinsTC - p.Tyr300Phe


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