Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06220 | A02 | 2631170 | C | T | missense_variant | MODERATE | c.3767G>A|p.Gly1256Glu |
S226 |
2 | BAA02g06220 | A02 | 2631874 | C | T | missense_variant | MODERATE | c.3403G>A|p.Glu1135Lys |
S278 |
3 | BAA02g06220 | A02 | 2632523 | G | A | missense_variant | MODERATE | c.2915C>T|p.Ser972Phe |
S266 |
4 | BAA02g06220 | A02 | 2633282 | C | T | synonymous_variant | LOW | c.2259G>A|p.Lys753Lys |
S116 |
5 | BAA02g06220 | A02 | 2634866 | C | T | synonymous_variant | LOW | c.1224G>A|p.Glu408Glu |
S278 |
6 | BAA02g06220 | A02 | 2635686 | G | A | missense_variant | MODERATE | c.736C>T|p.Arg246Cys |
S223 |
7 | BAA02g06220 | A02 | 2636126 | G | T | splice_region_variant&intron_variant | LOW | c.466-8C>A| |
S131 S196 S28 S49 |
8 | BAA02g06220 | A02 | 2636477 | C | T | missense_variant&splice_region_variant | MODERATE | c.275G>A|p.Arg92Lys |
S183 S198 |
9 | BAA02g06220 | A02 | 2636875 | C | T | missense_variant | MODERATE | c.71G>A|p.Arg24His |
S196 |
10 | BAA02g06220 | A02 | 2636895 | G | A | synonymous_variant | LOW | c.51C>T|p.Arg17Arg |
S10 |
11 | BAA02g06220 | A02 | 2636971 | G | A | upstream_gene_variant | MODIFIER | c.-26C>T| |
S126 |
12 | BAA02g06220 | A02 | 2637176 | C | T | upstream_gene_variant | MODIFIER | c.-231G>A| |
S87 |