Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g32980 | A01 | 21903067 | G | A | downstream_gene_variant | MODIFIER | c.*4561C>T| |
S280 |
2 | BAA01g32980 | A01 | 21904608 | G | A | downstream_gene_variant | MODIFIER | c.*3020C>T| |
S138 |
3 | BAA01g32980 | A01 | 21904693 | G | A | downstream_gene_variant | MODIFIER | c.*2935C>T| |
S124 |
4 | BAA01g32980 | A01 | 21904714 | G | A | downstream_gene_variant | MODIFIER | c.*2914C>T| |
S110 |
5 | BAA01g32980 | A01 | 21904822 | C | T | downstream_gene_variant | MODIFIER | c.*2806G>A| |
S269 |
6 | BAA01g32980 | A01 | 21907192 | C | T | downstream_gene_variant | MODIFIER | c.*436G>A| |
S25 S264 |
7 | BAA01g32980 | A01 | 21907253 | A | C | downstream_gene_variant | MODIFIER | c.*375T>G| |
S176 S242 S304 S47 S5 |
8 | BAA01g32980 | A01 | 21907870 | C | T | missense_variant | MODERATE | c.1003G>A|p.Glu335Lys |
S282 |
9 | BAA01g32980 | A01 | 21908217 | T | A | missense_variant | MODERATE | c.656A>T|p.Glu219Val |
S56 |
10 | BAA01g32980 | A01 | 21908234 | G | A | synonymous_variant | LOW | c.639C>T|p.Phe213Phe |
S65 |
11 | BAA01g32980 | A01 | 21908275 | C | T | missense_variant | MODERATE | c.598G>A|p.Gly200Arg |
S206 |
12 | BAA01g32980 | A01 | 21908533 | G | A | missense_variant | MODERATE | c.340C>T|p.Arg114Cys |
S35 |
13 | BAA01g32980 | A01 | 21908703 | G | A | missense_variant | MODERATE | c.170C>T|p.Thr57Ile |
S221 |
14 | BAA01g32980 | A01 | 21908797 | G | A | missense_variant | MODERATE | c.76C>T|p.Arg26Cys |
S107 |
15 | BAA01g32980 | A01 | 21911137 | C | T | upstream_gene_variant | MODIFIER | c.-2265G>A| |
S240 |
16 | BAA01g32980 | A01 | 21913769 | G | A | upstream_gene_variant | MODIFIER | c.-4897C>T| |
S138 |
17 | BAA01g32980 | A01 | 21913827 | G | A | upstream_gene_variant | MODIFIER | c.-4955C>T| |
S87 |