Variant #0000623437 (NC_000016.9:g.28890438G>T, NC_000016.9(NM_004320.4):c.136+1G>T (ATP2A1))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.28890438G>T |
DNA change (hg38) |
g.28879117G>T |
Published as |
ATP2A1(NM_004320.4):c.136+1G>T |
ISCN |
- |
DB-ID |
ATP2A1_000022 See all 2 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) |
Retrieve |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-06 12:43:26 +01:00 (CET) |
Date last edited |
2020-07-09 15:02:59 +02:00 (CEST) |

Variant on transcripts
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