Variant #0000000389 (NC_000012.11:g.112888151T>C, NM_002834.3:c.167T>C (PTPN11))
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.112888151T>C |
Reference |
- |
DB-ID |
PTPN11_000003 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Florian Bayersdorfer |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Florian Bayersdorfer |
Date created |
2023-07-18 10:37:45 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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