Variant #0000546484 (NC_000012.11:g.110760727C>A, NC_000012.11(NM_001681.3):c.464-70C>A (ATP2A2))
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.110760727C>A |
| DNA change (hg38) |
g.110322922C>A |
| Published as |
ATP2A2(NM_170665.3):c.464-70C>A (p.?), ATP2A2(NM_170665.4):c.464-70C>A |
| ISCN |
- |
| DB-ID |
ATP2A2_000294 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) |
Retrieve |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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