Variant #0000256033 (NC_000023.10:g.152807810A>C, ATP2B3(NM_021949.3):c.694A>C)

Chromosome X
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.152807810A>C
DNA change (hg38) g.153542352A>C
Published as ATP2B3(NM_001001344.2):c.694A>C (p.(Ile232Leu)), ATP2B3(NM_001001344.3):c.694A>C (p.I232L), ATP2B3(NM_021949.3):c.694A>C (p.I232L)
ISCN -
DB-ID ATP2B3_000086 See all 3 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) 0.00209 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.694A>C r.(?) p.(Ile232Leu)