Variant #0000006996 (NC_000017.11:g.7676154G>C, NM_000546.5:c.215C>G (TP53))
Individual ID |
00001252 |
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.7676154G>C |
Reference |
- |
DB-ID |
TP53_000001 See all 49 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Lina Nuñez-Private Practice |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-06-26 16:11:58 -03:00 (-03) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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