Variant #0000263287 (NC_000023.10:g.152807923G>C, ATP2B3(NM_021949.3):c.790+17G>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.152807923G>C
DNA change (hg38) g.153542465G>C
Published as ATP2B3(NM_021949.3):c.790+17G>C, ATP2B3(NM_021949.4):c.790+17G>C
ISCN -
DB-ID ATP2B3_000003 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) 0.99771 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.790+17G>C r.(=) p.(=)