Variant #0000989656 (NC_000010.10:g.52610567C>A, NC_000010.10(NM_014576.3):c.100-6685G>T (A1CF))
| Chromosome |
10 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.52610567C>A |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
A1CF_000088 |
| Frequency |
4/13006 |
| Freq. EA |
0/8600 |
| Freq. AA |
4/4406 |
| 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 16:30:47 +02:00 (CEST) |
| Date last edited |
2025-01-02 22:37:25 +01:00 (CET) |

Variant on transcripts
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