Variant #0000724397 (NC_000013.10:g.25946418C>G, ATP8A2(NM_016529.4):c.68C>G)

Chromosome 13
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.25946418C>G
DNA change (hg38) -
Published as ATP8A2(NM_016529.5):c.68C>G (p.S23W)
ISCN -
DB-ID ATP8A2_000044
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) 0.00023 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP8A2 NM_016529.4 ?/. - c.68C>G r.(?) p.(Ser23Trp)