Variant #0000001788 (NC_000019.9:g.40902114A>T, PRX(NM_181882.2):c.2145T>A)
Individual ID |
00001788 |
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.40902114A>T |
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_000006 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
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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