Variant #0001681404 (NC_000019.9:g.291276G>C, NC_000019.9(NM_003712.2):c.52+9C>G (PPAP2C))
Chromosome |
19 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.291276G>C |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
PPAP2C_000088 |
Frequency |
1/12932 |
Freq. EA |
1/8568 |
Freq. AA |
0/4364 |
Average frequency (gnomAD v.2.1.1) |
- |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Ivo F.A.C. Fokkema |
Date created |
2013-05-03 16:45:39 +02:00 (CEST) |
Date last edited |
2014-05-04 15:26:29 +02:00 (CEST) |

Variant on transcripts
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