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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