Variant #0000002635 (NC_000011.9:g.6638857C>T, TPP1(NM_000391.3):c.380G>A)
Individual ID |
00002635 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6638857C>T |
Reference |
Zhong et al. 2000 Genetics in Medicine 2: 312-318;Steinfeld et al. 2002 Am J Med Genet 112:347-353;P. Ray pers comm |
DB-ID |
TPP1_000009 |
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 |
Variant on transcripts
Screenings
|
|