Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15440 | A01 | 7444821 | C | T | upstream_gene_variant | MODIFIER | c.-4618C>T| |
S138 |
2 | BAA01g15440 | A01 | 7445622 | G | A | upstream_gene_variant | MODIFIER | c.-3817G>A| |
S192 |
3 | BAA01g15440 | A01 | 7446811 | G | A | upstream_gene_variant | MODIFIER | c.-2628G>A| |
S140 |
4 | BAA01g15440 | A01 | 7447632 | G | A | upstream_gene_variant | MODIFIER | c.-1807G>A| |
S94 |
5 | BAA01g15440 | A01 | 7447822 | G | A | upstream_gene_variant | MODIFIER | c.-1617G>A| |
S58 |
6 | BAA01g15440 | A01 | 7447880 | C | T | upstream_gene_variant | MODIFIER | c.-1559C>T| |
S226 |
7 | BAA01g15440 | A01 | 7448100 | C | T | upstream_gene_variant | MODIFIER | c.-1339C>T| |
S77 S82 |
8 | BAA01g15440 | A01 | 7448478 | G | A | upstream_gene_variant | MODIFIER | c.-961G>A| |
S297 |
9 | BAA01g15440 | A01 | 7448639 | G | A | upstream_gene_variant | MODIFIER | c.-800G>A| |
S149 |
10 | BAA01g15440 | A01 | 7449214 | C | T | upstream_gene_variant | MODIFIER | c.-225C>T| |
S10 |
11 | BAA01g15440 | A01 | 7450153 | G | A | missense_variant | MODERATE | c.280G>A|p.Glu94Lys |
S56 |
12 | BAA01g15440 | A01 | 7450381 | G | A | synonymous_variant | LOW | c.432G>A|p.Thr144Thr |
S305 |
13 | BAA01g15440 | A01 | 7450572 | G | A | synonymous_variant | LOW | c.534G>A|p.Lys178Lys |
S186 |
14 | BAA01g15440 | A01 | 7450664 | G | A | missense_variant | MODERATE | c.626G>A|p.Arg209His |
S217 S248 |
15 | BAA01g15440 | A01 | 7451218 | C | T | downstream_gene_variant | MODIFIER | c.*350C>T| |
S36 |
16 | BAA01g15440 | A01 | 7451515 | G | A | downstream_gene_variant | MODIFIER | c.*647G>A| |
S298 |