Variant #0000004404 (NC_000021.8:g.45194521_45194538del18, CSTB(NM_000100.3):c.168+1_168+18del18)
| Individual ID |
00004404 |
| Chromosome |
21 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45194521_45194538del18 |
| Reference |
Joensuu T1, Kuronen M, Alakurtti K, Tegelberg S, Hakala P, Aalto A, Huopaniemi L, Aula N, Michellucci R, Eriksson K, Lehesjoki AE.(2007) |
| DB-ID |
CSTB_000008 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Y Yang |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Y Yang |

Variant on transcripts
Screenings
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