Variant #0000985304 (NC_000001.10:g.160093018C>T, NM_000702.3:c.193C>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.160093018C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ATP1A2_000001 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121918619
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-05-16 14:38:01 +02:00 (CEST)
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.193C>T r.(?) p.(Arg65Trp)


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