Variant #0000002669 (NC_000011.9:g.6637307T>C, TPP1(NM_000391.3):c.1076-2A>G)
Individual ID |
00002669 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6637307T>C |
Reference |
Caillaud et al. 1999 Hum Genet 65 suppl:A232 |
DB-ID |
TPP1_000043 |
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 |
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Variant on transcripts
Screenings
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