Variant #0000919543 (NC_000001.10:g.160094128G>T, NM_000702.3:c.538G>T (ATP1A2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.160094128G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ATP1A2_000175
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1449406618
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-02-22 15:57:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP1A2 NM_000702.3 ?/. - c.538G>T r.(?) p.(Ala180Ser)


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