Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g21030 | A03 | 9478044 | G | A | missense_variant | MODERATE | c.919C>T|p.Pro307Ser |
S162 |
2 | BAA03g21030 | A03 | 9478170 | G | A | intron_variant | MODIFIER | c.814-21C>T| |
S229 |
3 | BAA03g21030 | A03 | 9479035 | G | A | intron_variant | MODIFIER | c.480-163C>T| |
S123 |
4 | BAA03g21030 | A03 | 9479395 | C | T | intron_variant | MODIFIER | c.480-523G>A| |
S265 |
5 | BAA03g21030 | A03 | 9479835 | C | T | intron_variant | MODIFIER | c.479+247G>A| |
S187 |
6 | BAA03g21030 | A03 | 9482026 | C | T | upstream_gene_variant | MODIFIER | c.-1466G>A| |
S173 |
7 | BAA03g21030 | A03 | 9482155 | A | G | upstream_gene_variant | MODIFIER | c.-1595T>C| |
S266 |
8 | BAA03g21030 | A03 | 9482171 | G | A | upstream_gene_variant | MODIFIER | c.-1611C>T| |
S206 S26 |
9 | BAA03g21030 | A03 | 9482449 | C | T | upstream_gene_variant | MODIFIER | c.-1889G>A| |
S82 S92 |
10 | BAA03g21030 | A03 | 9482611 | G | A | upstream_gene_variant | MODIFIER | c.-2051C>T| |
S14 |
11 | BAA03g21030 | A03 | 9482663 | G | A | upstream_gene_variant | MODIFIER | c.-2103C>T| |
S96 |
12 | BAA03g21030 | A03 | 9484134 | C | T | upstream_gene_variant | MODIFIER | c.-3574G>A| |
S80 |
13 | BAA03g21030 | A03 | 9484216 | C | T | upstream_gene_variant | MODIFIER | c.-3656G>A| |
S66 |
14 | BAA03g21030 | A03 | 9484399 | G | A | upstream_gene_variant | MODIFIER | c.-3839C>T| |
S104 S52 |
15 | BAA03g21030 | A03 | 9484498 | G | A | upstream_gene_variant | MODIFIER | c.-3938C>T| |
S189 |
16 | BAA03g21030 | A03 | 9484658 | G | A | upstream_gene_variant | MODIFIER | c.-4098C>T| |
S183 |
17 | BAA03g21030 | A03 | 9485026 | C | T | upstream_gene_variant | MODIFIER | c.-4466G>A| |
S131 |