Variant #0000438144 (NC_000001.10:g.160106455T>C, NM_000702.3:c.2659T>C (ATP1A2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.160106455T>C
DNA change (hg38) g.160136665T>C
Published as -
ISCN -
DB-ID ATP1A2_000024 See all 5 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 ?/? 19 c.2659T>C r.(?) p.Trp887Arg


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