Variant #0000007156 (NC_000019.10:g.1226530A>G, STK11(NM_000455.4):c.1185A>G)
Individual ID |
00001277 |
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Does not affect function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.1226530A>G |
Reference |
- |
DB-ID |
STK11_000012 |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Silvina Sisterna-Hospital de Comunidad |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Variant on transcripts
Screenings
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