Variant #0000263273 (NC_000023.10:g.152823728G>C, ATP2B3(NM_021949.3):c.2592G>C)

Chromosome X
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.152823728G>C
DNA change (hg38) g.153558270G>C
Published as ATP2B3(NM_021949.3):c.2592G>C (p.V864=), ATP2B3(NM_021949.4):c.2592G>C (p.V864=)
ISCN -
DB-ID ATP2B3_000011 See all 5 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) 0.54236 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     
ATP2B3 NM_021949.3 -/. - c.2592G>C r.(?) p.(Val864=)