Variant #0001467757 (NC_000016.9:g.16127038_16127039insC, NC_000016.9(NM_004996.3):c.677+11_677+12insC (ABCC1))
| Chromosome |
16 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.16127038_16127039insC |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
ABCC1_000034 |
| Frequency |
81/11680 |
| Freq. EA |
0/7932 |
| Freq. AA |
81/3748 |
| 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 16:42:42 +02:00 (CEST) |
| Date last edited |
2024-04-30 00:51:44 +02:00 (CEST) |

Variant on transcripts
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