Variant #0000000855 (NC_000017.10:g.3397646A>G, ASPA(NM_000049.2):c.637A>G)
Individual ID |
00000855 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.3397646A>G |
Reference |
Tacke U1, Olbrich H, Sass JO, Fekete A, Horvath J, Ziyeh S, Kleijer WJ, Rolland MO, Fisher S, Payne S, Vargiami E, Zafeiriou DI, Omran H.(2005) |
DB-ID |
ASPA_000039 See all 2 reported entries |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0.00023 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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