Variant #0000002657 (NC_000011.9:g.6637927C>A, TPP1(NM_000391.3):c.851G>T)
Individual ID |
00002657 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6637927C>A |
Reference |
Zhong et al. 2000 Genetics in Medicine 2: 312-318;Ju et al. 2002 J Med Genet 39:822-825Moore et al 2008 Clin Genet. 74:213-22 |
DB-ID |
TPP1_000031 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
1.0E-5 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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