Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35300 | A02 | 30330195 | C | T | upstream_gene_variant | MODIFIER | c.-634C>T| |
S289 S290 |
2 | BAA02g35300 | A02 | 30330368 | G | A | upstream_gene_variant | MODIFIER | c.-461G>A| |
S267 |
3 | BAA02g35300 | A02 | 30331433 | C | T | intron_variant | MODIFIER | c.360-38C>T| |
S19 |
4 | BAA02g35300 | A02 | 30332014 | C | T | missense_variant | MODERATE | c.637C>T|p.Leu213Phe |
S73 S91 |
5 | BAA02g35300 | A02 | 30332381 | G | A | intron_variant | MODIFIER | c.647+357G>A| |
S178 |
6 | BAA02g35300 | A02 | 30333101 | G | A | intron_variant | MODIFIER | c.647+1077G>A| |
S232 |
7 | BAA02g35300 | A02 | 30334808 | G | A | intron_variant | MODIFIER | c.647+2784G>A| |
S176 |
8 | BAA02g35300 | A02 | 30334912 | C | T | intron_variant | MODIFIER | c.647+2888C>T| |
S124 |
9 | BAA02g35300 | A02 | 30337721 | C | T | intron_variant | MODIFIER | c.648-2189C>T| |
S116 |
10 | BAA02g35300 | A02 | 30340816 | C | T | intron_variant | MODIFIER | c.929+386C>T| |
S284 |
11 | BAA02g35300 | A02 | 30340903 | C | T | intron_variant | MODIFIER | c.929+473C>T| |
S54 |
12 | BAA02g35300 | A02 | 30341747 | C | T | intron_variant | MODIFIER | c.1061+17C>T| |
S52 |
13 | BAA02g35300 | A02 | 30343120 | C | T | intron_variant | MODIFIER | c.1154+1092C>T| |
S212 |
14 | BAA02g35300 | A02 | 30343123 | G | A | intron_variant | MODIFIER | c.1154+1095G>A| |
S247 |
15 | BAA02g35300 | A02 | 30344671 | C | T | intron_variant | MODIFIER | c.1154+2643C>T| |
S266 |
16 | BAA02g35300 | A02 | 30345326 | G | C | intron_variant | MODIFIER | c.1155-2428G>C| |
S166 |
17 | BAA02g35300 | A02 | 30345861 | G | A | intron_variant | MODIFIER | c.1155-1893G>A| |
S47 |
18 | BAA02g35300 | A02 | 30346029 | C | T | intron_variant | MODIFIER | c.1155-1725C>T| |
S85 |
19 | BAA02g35300 | A02 | 30346856 | C | T | intron_variant | MODIFIER | c.1155-898C>T| |
S205 |
20 | BAA02g35300 | A02 | 30347188 | C | T | intron_variant | MODIFIER | c.1155-566C>T| |
S226 |
21 | BAA02g35300 | A02 | 30347500 | C | T | intron_variant | MODIFIER | c.1155-254C>T| |
S83 S88 |
22 | BAA02g35300 | A02 | 30347646 | G | A | intron_variant | MODIFIER | c.1155-108G>A| |
S215 |
23 | BAA02g35300 | A02 | 30347729 | C | T | intron_variant | MODIFIER | c.1155-25C>T| |
S202 |
24 | BAA02g35300 | A02 | 30348022 | G | A | missense_variant | MODERATE | c.1273G>A|p.Ala425Thr |
S302 |
25 | BAA02g35300 | A02 | 30348306 | C | T | synonymous_variant | LOW | c.1557C>T|p.Ile519Ile |
S112 |