Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16840 | A02 | 8317110 | G | A | upstream_gene_variant | MODIFIER | c.-3674G>A| |
S288 |
2 | BAA02g16840 | A02 | 8317246 | G | A | upstream_gene_variant | MODIFIER | c.-3538G>A| |
S122 |
3 | BAA02g16840 | A02 | 8317727 | G | A | upstream_gene_variant | MODIFIER | c.-3057G>A| |
S153 S213 |
4 | BAA02g16840 | A02 | 8318908 | C | T | upstream_gene_variant | MODIFIER | c.-1876C>T| |
S195 |
5 | BAA02g16840 | A02 | 8319682 | G | A | upstream_gene_variant | MODIFIER | c.-1102G>A| |
S93 |
6 | BAA02g16840 | A02 | 8319865 | C | T | upstream_gene_variant | MODIFIER | c.-919C>T| |
S262 |
7 | BAA02g16840 | A02 | 8319884 | C | T | upstream_gene_variant | MODIFIER | c.-900C>T| |
S138 |
8 | BAA02g16840 | A02 | 8319892 | C | T | upstream_gene_variant | MODIFIER | c.-892C>T| |
S107 |
9 | BAA02g16840 | A02 | 8320585 | C | T | upstream_gene_variant | MODIFIER | c.-199C>T| |
S18 |
10 | BAA02g16840 | A02 | 8320847 | C | T | synonymous_variant | LOW | c.64C>T|p.Leu22Leu |
S117 |
11 | BAA02g16840 | A02 | 8321710 | G | A | missense_variant | MODERATE | c.571G>A|p.Val191Met |
S110 |
12 | BAA02g16840 | A02 | 8322215 | C | T | missense_variant | MODERATE | c.731C>T|p.Ser244Phe |
S40 S49 |
13 | BAA02g16840 | A02 | 8322269 | G | A | missense_variant | MODERATE | c.785G>A|p.Gly262Glu |
S23 S303 |
14 | BAA02g16840 | A02 | 8322329 | G | A | missense_variant | MODERATE | c.845G>A|p.Gly282Asp |
S2 |
15 | BAA02g16840 | A02 | 8322597 | C | T | missense_variant | MODERATE | c.1019C>T|p.Ala340Val |
S192 |
16 | BAA02g16840 | A02 | 8323074 | G | A | downstream_gene_variant | MODIFIER | c.*236G>A| |
S23 |
17 | BAA02g16840 | A02 | 8324347 | C | T | downstream_gene_variant | MODIFIER | c.*1509C>T| |
S84 S93 |
18 | BAA02g16840 | A02 | 8324991 | G | A | downstream_gene_variant | MODIFIER | c.*2153G>A| |
S149 S190 |
19 | BAA02g16840 | A02 | 8327340 | G | A | downstream_gene_variant | MODIFIER | c.*4502G>A| |
S69 |
20 | BAA02g16840 | A02 | 8327655 | C | T | downstream_gene_variant | MODIFIER | c.*4817C>T| |
S100 |