Variant #0000001789 (NC_000019.9:g.40904661delG, PRX(NM_181882.2):c.247delC)
| Individual ID |
00001789 |
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.40904661delG |
| Reference |
Takashima H1, Boerkoel CF, De Jonghe P, Ceuterick C, Martin JJ, Voit T, Schr?der JM, Williams A, Brophy PJ, Timmerman V, Lupski JR.(2002) |
| DB-ID |
PRX_000007 |
| 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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