Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g06800 | A04 | 4504861 | C | T | upstream_gene_variant | MODIFIER | c.-4138C>T| |
S233 |
2 | BAA04g06800 | A04 | 4505055 | G | A | upstream_gene_variant | MODIFIER | c.-3944G>A| |
S34 |
3 | BAA04g06800 | A04 | 4505185 | G | A | upstream_gene_variant | MODIFIER | c.-3814G>A| |
S108 |
4 | BAA04g06800 | A04 | 4505443 | T | G | upstream_gene_variant | MODIFIER | c.-3556T>G| |
S157 S163 S249 |
5 | BAA04g06800 | A04 | 4505462 | C | T | upstream_gene_variant | MODIFIER | c.-3537C>T| |
S25 S264 |
6 | BAA04g06800 | A04 | 4506765 | G | A | upstream_gene_variant | MODIFIER | c.-2234G>A| |
S150 |
7 | BAA04g06800 | A04 | 4507039 | C | T | upstream_gene_variant | MODIFIER | c.-1960C>T| |
S1 S90 |
8 | BAA04g06800 | A04 | 4507059 | G | A | upstream_gene_variant | MODIFIER | c.-1940G>A| |
S181 |
9 | BAA04g06800 | A04 | 4507063 | G | A | upstream_gene_variant | MODIFIER | c.-1936G>A| |
S60 |
10 | BAA04g06800 | A04 | 4507362 | C | T | upstream_gene_variant | MODIFIER | c.-1637C>T| |
S155 S211 |
11 | BAA04g06800 | A04 | 4507588 | G | A | upstream_gene_variant | MODIFIER | c.-1411G>A| |
S136 |
12 | BAA04g06800 | A04 | 4507877 | C | T | upstream_gene_variant | MODIFIER | c.-1122C>T| |
S32 |
13 | BAA04g06800 | A04 | 4507965 | C | T | upstream_gene_variant | MODIFIER | c.-1034C>T| |
S210 |
14 | BAA04g06800 | A04 | 4508234 | G | A | upstream_gene_variant | MODIFIER | c.-765G>A| |
S5 |
15 | BAA04g06800 | A04 | 4508287 | C | T | upstream_gene_variant | MODIFIER | c.-712C>T| |
S180 |
16 | BAA04g06800 | A04 | 4509028 | C | T | synonymous_variant | LOW | c.30C>T|p.Phe10Phe |
S295 |
17 | BAA04g06800 | A04 | 4509846 | G | A | missense_variant | MODERATE | c.848G>A|p.Gly283Asp |
S124 |
18 | BAA04g06800 | A04 | 4509898 | C | T | synonymous_variant | LOW | c.900C>T|p.Leu300Leu |
S205 |
19 | BAA04g06800 | A04 | 4510287 | C | T | missense_variant | MODERATE | c.1141C>T|p.Pro381Ser |
S200 |
20 | BAA04g06800 | A04 | 4510700 | C | T | missense_variant | MODERATE | c.1295C>T|p.Ser432Phe |
S238 S8 |
21 | BAA04g06800 | A04 | 4510733 | G | A | missense_variant | MODERATE | c.1328G>A|p.Gly443Asp |
S56 |
22 | BAA04g06800 | A04 | 4510740 | C | T | synonymous_variant | LOW | c.1335C>T|p.Val445Val |
S274 |
23 | BAA04g06800 | A04 | 4510967 | G | A | synonymous_variant | LOW | c.1425G>A|p.Val475Val |
S126 |
24 | BAA04g06800 | A04 | 4511349 | G | A | downstream_gene_variant | MODIFIER | c.*235G>A| |
S144 |
25 | BAA04g06800 | A04 | 4512223 | C | T | downstream_gene_variant | MODIFIER | c.*1109C>T| |
S100 |