Variant #0000654753 (NC_000003.11:g.10452400C>T, NM_001683.3:c.299G>A (ATP2B2))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.10452400C>T |
DNA change (hg38) |
g.10410716C>T |
Published as |
ATP2B2(NM_001330611.2):c.299G>A (p.W100*) |
ISCN |
- |
DB-ID |
ATP2B2_000031 |
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) |
Retrieve |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2020-06-12 12:00:17 +02:00 (CEST) |

Variant on transcripts
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