Variant #0000438138 (NC_000001.10:g.160105036G>A, NM_000702.3:c.2066G>A (ATP1A2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.160105036G>A
DNA change (hg38) g.160135246G>A
Published as -
ISCN -
DB-ID ATP1A2_000015 See all 23 reported entries
Variant remarks tested expression in vitro
Reference PubMed: Capendeguy 2004
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Paola Carrera
Database submission license No license selected
Created by Paola Carrera
Date created 2008-06-26 18:00:08 +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     
ATP1A2 NM_000702.3 +?/+? 15 c.2066G>A r.(?) p.Arg689Gln


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