Variant #0000002456 (NC_000007.13:g.143042856G>T, CLCN1(NM_000083.2):c.2172+1G>T)
| Individual ID |
00002456 |
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.143042856G>T |
| Reference |
Chen L1, Schaerer M, Lu ZH, Lang D, Joncourt F, Weis J, Fritschi J, Kappeler L, Gallati S, Sigel E, Burgunder JM.(2004) |
| DB-ID |
CLCN1_000090 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| 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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