Variant #0000623437 (NC_000016.9:g.28890438G>T, NM_015503.2:c.*5652G>T (SH2B1))
| 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
|