Variant #0000085706 (NC_000003.11:g.130649329delinsN[24], NM_001001486.1:c.76delGins~24 (ATP2C1))
Individual ID |
00055738 |
Chromosome |
3 |
Allele |
Parent #1 |
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.130649329delinsN[24] |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
ATP2C1_000116 |
Variant remarks |
- |
Reference |
PubMed: Fairclough 2004 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Michel van Geel |
Date created |
2012-01-29 21:11:29 +01:00 (CET) |
Date last edited |
2021-12-13 16:51:37 +01:00 (CET) |

Variant on transcripts
Screenings
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