Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21110 | A02 | 11295945 | G | A | upstream_gene_variant | MODIFIER | c.-4400G>A| |
S47 |
2 | BAA02g21110 | A02 | 11296450 | G | A | upstream_gene_variant | MODIFIER | c.-3895G>A| |
S58 |
3 | BAA02g21110 | A02 | 11296511 | G | A | upstream_gene_variant | MODIFIER | c.-3834G>A| |
S238 |
4 | BAA02g21110 | A02 | 11296963 | G | A | upstream_gene_variant | MODIFIER | c.-3382G>A| |
S192 |
5 | BAA02g21110 | A02 | 11297533 | C | T | upstream_gene_variant | MODIFIER | c.-2812C>T| |
S226 |
6 | BAA02g21110 | A02 | 11297969 | G | A | upstream_gene_variant | MODIFIER | c.-2376G>A| |
S202 |
7 | BAA02g21110 | A02 | 11298186 | G | A | upstream_gene_variant | MODIFIER | c.-2159G>A| |
S217 S248 |
8 | BAA02g21110 | A02 | 11298227 | G | A | upstream_gene_variant | MODIFIER | c.-2118G>A| |
S7 |
9 | BAA02g21110 | A02 | 11300745 | C | T | missense_variant | MODERATE | c.287C>T|p.Ala96Val |
S9 |
10 | BAA02g21110 | A02 | 11302096 | C | T | synonymous_variant | LOW | c.531C>T|p.Asp177Asp |
S53 |
11 | BAA02g21110 | A02 | 11302106 | G | A | missense_variant | MODERATE | c.541G>A|p.Glu181Lys |
S291 |
12 | BAA02g21110 | A02 | 11302113 | G | A | missense_variant | MODERATE | c.548G>A|p.Arg183Lys |
S10 |