Variant #0000002666 (NC_000011.9:g.6637564T>G, TPP1(NM_000391.3):c.1057A>C)
Individual ID |
00002666 |
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6637564T>G |
Reference |
Steinfeld et al. 2002 Am J Med Geent 112:347-354 |
DB-ID |
TPP1_000040 |
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
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