Variant #0010491695 (NC_000017.10:g.35307498C>T, NC_000017.10(NM_012138.3):c.92-16C>T (AATF))
| Chromosome |
17 |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.35307498C>T |
| DB-ID |
- |
| dbSNP ID |
- |
| gnomAD frequency |
1/244722 |
| gnomAD homozygote count |
0/122360 |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Database submission license |
No license selected |
| Created by |
LOVD |
| Date created |
2017-02-27 00:00:00 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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