Variant #0000503926 (NC_000001.10:g.160090708T>A, NM_000702.3:c.25T>A (ATP1A2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.160090708T>A
DNA change (hg38) g.160120918T>A
Published as ATP1A2(NM_000702.2):c.25T>A (p.Y9N), ATP1A2(NM_000702.3):c.25T>A (p.(Tyr9Asn)), ATP1A2(NM_000702.4):c.25T>A (p.Y9N)
ISCN -
DB-ID ATP1A2_000066 See all 7 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00168 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +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 -?/. - c.25T>A r.(?) p.(Tyr9Asn)


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