Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07630 | A10 | 4605081 | G | A | upstream_gene_variant | MODIFIER | c.-2777G>A| |
S128 |
2 | BAA10g07630 | A10 | 4607594 | G | A | upstream_gene_variant | MODIFIER | c.-264G>A| |
S277 |
3 | BAA10g07630 | A10 | 4607708 | C | T | upstream_gene_variant | MODIFIER | c.-150C>T| |
S282 |
4 | BAA10g07630 | A10 | 4607966 | G | A | missense_variant | MODERATE | c.109G>A|p.Glu37Lys |
S289 |
5 | BAA10g07630 | A10 | 4608115 | G | A | synonymous_variant | LOW | c.258G>A|p.Leu86Leu |
S62 |
6 | BAA10g07630 | A10 | 4609621 | C | T | downstream_gene_variant | MODIFIER | c.*173C>T| |
S224 |
7 | BAA10g07630 | A10 | 4610219 | C | T | downstream_gene_variant | MODIFIER | c.*771C>T| |
S159 S187 S243 S298 S299 |
8 | BAA10g07630 | A10 | 4610683 | G | A | downstream_gene_variant | MODIFIER | c.*1235G>A| |
S55 |
9 | BAA10g07630 | A10 | 4610742 | C | T | downstream_gene_variant | MODIFIER | c.*1294C>T| |
S176 |
10 | BAA10g07630 | A10 | 4610987 | G | A | downstream_gene_variant | MODIFIER | c.*1539G>A| |
S69 |
11 | BAA10g07630 | A10 | 4611456 | C | T | downstream_gene_variant | MODIFIER | c.*2008C>T| |
S305 |
12 | BAA10g07630 | A10 | 4611467 | G | A | downstream_gene_variant | MODIFIER | c.*2019G>A| |
S9 |
13 | BAA10g07630 | A10 | 4611933 | C | T | downstream_gene_variant | MODIFIER | c.*2485C>T| |
S41 |
14 | BAA10g07630 | A10 | 4612492 | G | A | downstream_gene_variant | MODIFIER | c.*3044G>A| |
S95 |
15 | BAA10g07630 | A10 | 4612894 | C | T | downstream_gene_variant | MODIFIER | c.*3446C>T| |
S193 |
16 | BAA10g07630 | A10 | 4613384 | C | T | downstream_gene_variant | MODIFIER | c.*3936C>T| |
S19 |
17 | BAA10g07630 | A10 | 4613924 | C | T | downstream_gene_variant | MODIFIER | c.*4476C>T| |
S133 |