Variant #0000001146 (NC_000019.9:g.42474685A>C, ATP1A3(NM_152296.4):c.2273T>G)
| Individual ID |
00001146 |
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42474685A>C |
| Reference |
Oblak AL1, Hagen MC, Sweadner KJ, Haq I, Whitlow CT, Maldjian JA, Epperson F, Cook JF, Stacy M, Murrell JR, Ozelius LJ, Brashear A, Ghetti B.(2014) |
| DB-ID |
ATP1A3_000004 See all 2 reported entries |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Y Yang |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Y Yang |

Variant on transcripts
Screenings
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