Variant #0000263239 (NC_000001.10:g.17326540G>A, NM_022089.2:c.1005C>T (ATP13A2))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17326540G>A
DNA change (hg38) g.17000045G>A
Published as ATP13A2(NM_022089.2):c.1005C>T (p.A335=), ATP13A2(NM_022089.4):c.1005C>T (p.A335=)
ISCN -
DB-ID ATP13A2_000043 See all 4 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) 0.02624 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP13A2 NM_022089.2 -/. - c.1005C>T r.(?) p.(Ala335=)


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