Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14680 | A10 | 15316573 | C | T | upstream_gene_variant | MODIFIER | c.-3789C>T| |
S282 |
2 | BAA10g14680 | A10 | 15317189 | T | A | upstream_gene_variant | MODIFIER | c.-3173T>A| |
S113 S118 |
3 | BAA10g14680 | A10 | 15317277 | G | A | upstream_gene_variant | MODIFIER | c.-3085G>A| |
S109 |
4 | BAA10g14680 | A10 | 15318224 | C | T | upstream_gene_variant | MODIFIER | c.-2138C>T| |
S199 |
5 | BAA10g14680 | A10 | 15318601 | G | A | upstream_gene_variant | MODIFIER | c.-1761G>A| |
S293 |
6 | BAA10g14680 | A10 | 15319115 | G | A | upstream_gene_variant | MODIFIER | c.-1247G>A| |
S198 |
7 | BAA10g14680 | A10 | 15319617 | G | A | upstream_gene_variant | MODIFIER | c.-745G>A| |
S65 |
8 | BAA10g14680 | A10 | 15320484 | G | A | synonymous_variant | LOW | c.123G>A|p.Glu41Glu |
S255 |
9 | BAA10g14680 | A10 | 15320525 | C | T | missense_variant | MODERATE | c.164C>T|p.Thr55Ile |
S76 |
10 | BAA10g14680 | A10 | 15321104 | C | T | intron_variant | MODIFIER | c.541+114C>T| |
S168 |
11 | BAA10g14680 | A10 | 15321511 | G | A | downstream_gene_variant | MODIFIER | c.*39G>A| |
S192 |
12 | BAA10g14680 | A10 | 15321577 | C | T | downstream_gene_variant | MODIFIER | c.*105C>T| |
S190 |
13 | BAA10g14680 | A10 | 15321637 | C | T | downstream_gene_variant | MODIFIER | c.*165C>T| |
S281 |
14 | BAA10g14680 | A10 | 15323524 | C | T | downstream_gene_variant | MODIFIER | c.*2052C>T| |
S61 |