Variant #0000002646 (NC_000011.9:g.6638271G>A, TPP1(NM_000391.3):c.622C>T)
Individual ID |
00002646 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6638271G>A |
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 |
DB-ID |
TPP1_000020 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0.00024 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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