Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14240 | A10 | 15040724 | G | A | upstream_gene_variant | MODIFIER | c.-4598G>A| |
S90 |
2 | BAA10g14240 | A10 | 15041011 | C | T | upstream_gene_variant | MODIFIER | c.-4311C>T| |
S10 |
3 | BAA10g14240 | A10 | 15041117 | G | A | upstream_gene_variant | MODIFIER | c.-4205G>A| |
S62 |
4 | BAA10g14240 | A10 | 15041489 | C | T | upstream_gene_variant | MODIFIER | c.-3833C>T| |
S249 |
5 | BAA10g14240 | A10 | 15041512 | C | T | upstream_gene_variant | MODIFIER | c.-3810C>T| |
S283 |
6 | BAA10g14240 | A10 | 15041533 | C | T | upstream_gene_variant | MODIFIER | c.-3789C>T| |
S63 |
7 | BAA10g14240 | A10 | 15042013 | C | T | upstream_gene_variant | MODIFIER | c.-3309C>T| |
S187 |
8 | BAA10g14240 | A10 | 15043567 | C | T | upstream_gene_variant | MODIFIER | c.-1755C>T| |
S206 |
9 | BAA10g14240 | A10 | 15045697 | C | T | stop_gained | HIGH | c.376C>T|p.Gln126* |
S45 |
10 | BAA10g14240 | A10 | 15045873 | G | A | synonymous_variant | LOW | c.552G>A|p.Pro184Pro |
S67 |
11 | BAA10g14240 | A10 | 15046595 | C | T | missense_variant | MODERATE | c.1193C>T|p.Ala398Val |
S210 |
12 | BAA10g14240 | A10 | 15049217 | C | T | downstream_gene_variant | MODIFIER | c.*1936C>T| |
S46 |
13 | BAA10g14240 | A10 | 15049704 | C | T | downstream_gene_variant | MODIFIER | c.*2423C>T| |
S78 S83 |
14 | BAA10g14240 | A10 | 15050455 | C | T | downstream_gene_variant | MODIFIER | c.*3174C>T| |
S246 |