Variant #0000002635 (NC_000011.9:g.6638857C>T, TPP1(NM_000391.3):c.380G>A)
| Individual ID |
00002635 |
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6638857C>T |
| Reference |
Zhong et al. 2000 Genetics in Medicine 2: 312-318;Steinfeld et al. 2002 Am J Med Genet 112:347-353;P. Ray pers comm |
| DB-ID |
TPP1_000009 |
| 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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