Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00170 | A10 | 76607 | C | T | downstream_gene_variant | MODIFIER | c.*907G>A| |
S28 |
2 | BAA10g00170 | A10 | 76684 | G | A | downstream_gene_variant | MODIFIER | c.*830C>T| |
S64 |
3 | BAA10g00170 | A10 | 77062 | G | A | downstream_gene_variant | MODIFIER | c.*452C>T| |
S283 |
4 | BAA10g00170 | A10 | 78418 | C | T | intron_variant | MODIFIER | c.2520+37G>A| |
S124 S259 |
5 | BAA10g00170 | A10 | 78442 | C | T | intron_variant | MODIFIER | c.2520+13G>A| |
S62 |
6 | BAA10g00170 | A10 | 78484 | C | T | missense_variant | MODERATE | c.2491G>A|p.Ala831Thr |
S202 |
7 | BAA10g00170 | A10 | 80528 | C | T | missense_variant | MODERATE | c.1682G>A|p.Gly561Glu |
S181 |
8 | BAA10g00170 | A10 | 80598 | G | A | missense_variant | MODERATE | c.1612C>T|p.His538Tyr |
S255 |
9 | BAA10g00170 | A10 | 81407 | G | A | synonymous_variant | LOW | c.987C>T|p.Pro329Pro |
S263 S288 |
10 | BAA10g00170 | A10 | 82729 | C | T | upstream_gene_variant | MODIFIER | c.-336G>A| |
S108 |
11 | BAA10g00170 | A10 | 82938 | C | T | upstream_gene_variant | MODIFIER | c.-545G>A| |
S27 |
12 | BAA10g00170 | A10 | 87157 | C | T | upstream_gene_variant | MODIFIER | c.-4764G>A| |
S161 S228 S244 S290 |