Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13000 | A02 | 5808025 | G | A | missense_variant | MODERATE | c.2776C>T|p.Arg926Trp |
S231 |
2 | BAA02g13000 | A02 | 5808565 | C | T | missense_variant | MODERATE | c.2236G>A|p.Asp746Asn |
S139 |
3 | BAA02g13000 | A02 | 5808855 | C | T | missense_variant | MODERATE | c.1946G>A|p.Arg649Lys |
S179 |
4 | BAA02g13000 | A02 | 5808945 | C | T | missense_variant | MODERATE | c.1856G>A|p.Gly619Glu |
S58 |
5 | BAA02g13000 | A02 | 5809026 | G | A | missense_variant | MODERATE | c.1775C>T|p.Ala592Val |
S282 |
6 | BAA02g13000 | A02 | 5809123 | G | A | missense_variant | MODERATE | c.1678C>T|p.Leu560Phe |
S263 |
7 | BAA02g13000 | A02 | 5809204 | C | T | missense_variant | MODERATE | c.1597G>A|p.Gly533Arg |
S25 |
8 | BAA02g13000 | A02 | 5809438 | C | T | missense_variant | MODERATE | c.1363G>A|p.Glu455Lys |
S124 |
9 | BAA02g13000 | A02 | 5809693 | C | T | missense_variant | MODERATE | c.1207G>A|p.Asp403Asn |
S224 |
10 | BAA02g13000 | A02 | 5810231 | C | T | missense_variant | MODERATE | c.742G>A|p.Glu248Lys |
S13 |
11 | BAA02g13000 | A02 | 5810427 | C | T | synonymous_variant | LOW | c.546G>A|p.Thr182Thr |
S276 |
12 | BAA02g13000 | A02 | 5810891 | C | T | missense_variant | MODERATE | c.82G>A|p.Ala28Thr |
S186 |
13 | BAA02g13000 | A02 | 5811649 | G | A | upstream_gene_variant | MODIFIER | c.-677C>T| |
S271 |
14 | BAA02g13000 | A02 | 5811656 | C | T | upstream_gene_variant | MODIFIER | c.-684G>A| |
S224 |
15 | BAA02g13000 | A02 | 5812159 | G | A | upstream_gene_variant | MODIFIER | c.-1187C>T| |
S193 |
16 | BAA02g13000 | A02 | 5813250 | C | T | upstream_gene_variant | MODIFIER | c.-2278G>A| |
S178 |
17 | BAA02g13000 | A02 | 5813252 | C | T | upstream_gene_variant | MODIFIER | c.-2280G>A| |
S107 |
18 | BAA02g13000 | A02 | 5813350 | G | A | upstream_gene_variant | MODIFIER | c.-2378C>T| |
S134 |
19 | BAA02g13000 | A02 | 5813942 | G | A | upstream_gene_variant | MODIFIER | c.-2970C>T| |
S136 |
20 | BAA02g13000 | A02 | 5813996 | G | A | upstream_gene_variant | MODIFIER | c.-3024C>T| |
S69 |