Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g05740 | A04 | 3722678 | G | A | stop_gained | HIGH | c.364C>T|p.Gln122* |
S94 |
2 | BAA04g05740 | A04 | 3722823 | C | T | intron_variant | MODIFIER | c.324-105G>A| |
S135 |
3 | BAA04g05740 | A04 | 3722941 | G | A | intron_variant | MODIFIER | c.323+26C>T| |
S201 |
4 | BAA04g05740 | A04 | 3722951 | G | A | intron_variant | MODIFIER | c.323+16C>T| |
S166 |
5 | BAA04g05740 | A04 | 3723330 | G | A | intron_variant | MODIFIER | c.175-9C>T| |
S177 |
6 | BAA04g05740 | A04 | 3723950 | G | A | upstream_gene_variant | MODIFIER | c.-376C>T| |
S278 |
7 | BAA04g05740 | A04 | 3724901 | C | T | upstream_gene_variant | MODIFIER | c.-1327G>A| |
S46 |
8 | BAA04g05740 | A04 | 3727756 | C | T | upstream_gene_variant | MODIFIER | c.-4182G>A| |
S192 |
9 | BAA04g05740 | A04 | 3727862 | C | T | upstream_gene_variant | MODIFIER | c.-4288G>A| |
S286 |
10 | BAA04g05740 | A04 | 3727929 | C | T | upstream_gene_variant | MODIFIER | c.-4355G>A| |
S247 |
11 | BAA04g05740 | A04 | 3727932 | G | A | upstream_gene_variant | MODIFIER | c.-4358C>T| |
S273 |