Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04120 | A10 | 2008378 | A | T | downstream_gene_variant | MODIFIER | c.*2586T>A| |
S1 |
2 | BAA10g04120 | A10 | 2008997 | C | T | downstream_gene_variant | MODIFIER | c.*1967G>A| |
S233 |
3 | BAA10g04120 | A10 | 2010375 | G | A | downstream_gene_variant | MODIFIER | c.*589C>T| |
S241 S242 |
4 | BAA10g04120 | A10 | 2010599 | C | T | downstream_gene_variant | MODIFIER | c.*365G>A| |
S249 |
5 | BAA10g04120 | A10 | 2011813 | C | T | missense_variant | MODERATE | c.664G>A|p.Ala222Thr |
S202 |
6 | BAA10g04120 | A10 | 2012333 | G | A | missense_variant | MODERATE | c.461C>T|p.Ser154Phe |
S138 |
7 | BAA10g04120 | A10 | 2013132 | G | A | upstream_gene_variant | MODIFIER | c.-251C>T| |
S280 |
8 | BAA10g04120 | A10 | 2013512 | G | A | upstream_gene_variant | MODIFIER | c.-631C>T| |
S45 |
9 | BAA10g04120 | A10 | 2015639 | G | A | upstream_gene_variant | MODIFIER | c.-2758C>T| |
S133 |
10 | BAA10g04120 | A10 | 2015843 | G | A | upstream_gene_variant | MODIFIER | c.-2962C>T| |
S133 |
11 | BAA10g04120 | A10 | 2017105 | G | T | upstream_gene_variant | MODIFIER | c.-4224C>A| |
S135 |
12 | BAA10g04120 | A10 | 2017286 | G | A | upstream_gene_variant | MODIFIER | c.-4405C>T| |
S112 |
13 | BAA10g04120 | A10 | 2017751 | C | T | upstream_gene_variant | MODIFIER | c.-4870G>A| |
S203 |