Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01350 | A09 | 996420 | C | T | missense_variant | MODERATE | c.2203G>A|p.Gly735Arg |
S246 |
2 | BAA09g01350 | A09 | 996441 | G | A | missense_variant | MODERATE | c.2182C>T|p.Arg728Cys |
S201 |
3 | BAA09g01350 | A09 | 996719 | C | T | missense_variant | MODERATE | c.1904G>A|p.Arg635Lys |
S234 |
4 | BAA09g01350 | A09 | 997601 | G | A | missense_variant | MODERATE | c.1022C>T|p.Ser341Phe |
S153 S213 |
5 | BAA09g01350 | A09 | 997920 | C | T | missense_variant | MODERATE | c.703G>A|p.Ala235Thr |
S115 |
6 | BAA09g01350 | A09 | 998273 | G | A | missense_variant | MODERATE | c.440C>T|p.Ala147Val |
S295 |
7 | BAA09g01350 | A09 | 998286 | C | T | missense_variant | MODERATE | c.427G>A|p.Glu143Lys |
S117 S84 S93 |
8 | BAA09g01350 | A09 | 998475 | G | A | missense_variant | MODERATE | c.238C>T|p.Pro80Ser |
S197 |
9 | BAA09g01350 | A09 | 998478 | G | A | missense_variant | MODERATE | c.235C>T|p.Pro79Ser |
S192 |
10 | BAA09g01350 | A09 | 998505 | C | T | missense_variant | MODERATE | c.208G>A|p.Gly70Arg |
S71 |
11 | BAA09g01350 | A09 | 1000589 | G | A | upstream_gene_variant | MODIFIER | c.-1877C>T| |
S190 |
12 | BAA09g01350 | A09 | 1000630 | G | A | upstream_gene_variant | MODIFIER | c.-1918C>T| |
S30 S31 |
13 | BAA09g01350 | A09 | 1000683 | G | A | upstream_gene_variant | MODIFIER | c.-1971C>T| |
S188 |
14 | BAA09g01350 | A09 | 1001242 | C | T | upstream_gene_variant | MODIFIER | c.-2530G>A| |
S303 |
15 | BAA09g01350 | A09 | 1002128 | G | A | upstream_gene_variant | MODIFIER | c.-3416C>T| |
S114 |