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 International |
Created by |
VKGL-NL_Rotterdam |

Variant on transcripts
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