Variant #0000946940 (NC_000001.10:g.116927468T>C, NC_000001.10(NM_000701.7):c.183+4T>C (ATP1A1))

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.116927468T>C
DNA change (hg38) -
Published as ATP1A1(NM_001160233.1):c.183+4T>C, ATP1A1(NM_001160233.2):c.183+4T>C
ISCN -
DB-ID ATP1A1_000024 See all 2 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) 0.00304 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +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     
ATP1A1 NM_000701.7 -?/. - c.183+4T>C r.spl? p.?


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