Variant #0001291374 (NC_000013.10:g.95862896A>G, NC_000013.10(NM_005845.3):c.621+50T>C (ABCC4))
| Chromosome |
13 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.95862896A>G |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
ABCC4_000247 |
| Frequency |
9681/13006 |
| Freq. EA |
6982/8600 |
| Freq. AA |
2699/4406 |
| 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 16:41:01 +02:00 (CEST) |
| Date last edited |
2024-12-14 20:26:26 +01:00 (CET) |

Variant on transcripts
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