Variant #0000002634 (NC_000011.9:g.6638926A>T, TPP1(NM_000391.3):c.311T>A)
| Individual ID |
00002634 |
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6638926A>T |
| Reference |
Kohan et al. 2008. Human Genetics 123: 537-555 (553);Kohan et al 2009 Clin Genet 76: 372-382;Moore et al 2008 Clin Genet. 74:213-22 |
| DB-ID |
TPP1_000008 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0 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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