Variant #0000002641 (NC_000011.9:g.6638385C>G, TPP1(NM_000391.3):c.509-1G>C)
| Individual ID |
00002641 |
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6638385C>G |
| Reference |
Sleat et al. 1997 Science 277:1802-1805;Zhong et al. 1998 Clin Genet 54:234-238;Sleat et al. 1999 Am J Hum Genet 64:1511-1523;Hartikainen et al. 1999 Mol Genet Mab 67:162-168;Caillaud et al. 1999 Hum Genet 65 suppl:A232 |
| DB-ID |
TPP1_000015 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00041 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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