Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g23160 | A01 | 11862902 | G | A | upstream_gene_variant | MODIFIER | c.-4749G>A| |
S155 S211 |
2 | BAA01g23160 | A01 | 11863363 | C | T | upstream_gene_variant | MODIFIER | c.-4288C>T| |
S36 |
3 | BAA01g23160 | A01 | 11863452 | G | A | upstream_gene_variant | MODIFIER | c.-4199G>A| |
S75 S81 |
4 | BAA01g23160 | A01 | 11864955 | C | T | upstream_gene_variant | MODIFIER | c.-2696C>T| |
S231 |
5 | BAA01g23160 | A01 | 11865862 | G | A | upstream_gene_variant | MODIFIER | c.-1789G>A| |
S245 |
6 | BAA01g23160 | A01 | 11867640 | G | A | upstream_gene_variant | MODIFIER | c.-11G>A| |
S33 |
7 | BAA01g23160 | A01 | 11868008 | G | A | missense_variant | MODERATE | c.358G>A|p.Glu120Lys |
S293 |
8 | BAA01g23160 | A01 | 11868189 | C | T | missense_variant | MODERATE | c.539C>T|p.Pro180Leu |
S192 |
9 | BAA01g23160 | A01 | 11868471 | C | T | missense_variant | MODERATE | c.821C>T|p.Thr274Ile |
S36 |
10 | BAA01g23160 | A01 | 11868662 | C | T | missense_variant | MODERATE | c.1012C>T|p.Leu338Phe |
S25 |
11 | BAA01g23160 | A01 | 11868705 | G | A | missense_variant | MODERATE | c.1055G>A|p.Arg352His |
S246 |
12 | BAA01g23160 | A01 | 11868869 | G | A | missense_variant | MODERATE | c.1219G>A|p.Gly407Arg |
S45 |