Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g01780 | Scaffold13 | 14601170 | C | T | upstream_gene_variant | MODIFIER | c.-4439C>T| |
S289 S290 |
2 | BAS13g01780 | Scaffold13 | 14601433 | C | T | upstream_gene_variant | MODIFIER | c.-4176C>T| |
S90 |
3 | BAS13g01780 | Scaffold13 | 14601543 | G | A | upstream_gene_variant | MODIFIER | c.-4066G>A| |
S157 |
4 | BAS13g01780 | Scaffold13 | 14603007 | C | T | upstream_gene_variant | MODIFIER | c.-2602C>T| |
S269 |
5 | BAS13g01780 | Scaffold13 | 14603209 | G | A | upstream_gene_variant | MODIFIER | c.-2400G>A| |
S35 |
6 | BAS13g01780 | Scaffold13 | 14603270 | C | T | upstream_gene_variant | MODIFIER | c.-2339C>T| |
S291 |
7 | BAS13g01780 | Scaffold13 | 14603517 | C | T | upstream_gene_variant | MODIFIER | c.-2092C>T| |
S250 |
8 | BAS13g01780 | Scaffold13 | 14604912 | G | A | upstream_gene_variant | MODIFIER | c.-697G>A| |
S191 |
9 | BAS13g01780 | Scaffold13 | 14605130 | G | A | upstream_gene_variant | MODIFIER | c.-479G>A| |
S110 |
10 | BAS13g01780 | Scaffold13 | 14605573 | G | A | upstream_gene_variant | MODIFIER | c.-36G>A| |
S281 |
11 | BAS13g01780 | Scaffold13 | 14605763 | C | T | missense_variant | MODERATE | c.155C>T|p.Pro52Leu |
S111 |
12 | BAS13g01780 | Scaffold13 | 14605866 | G | A | synonymous_variant | LOW | c.258G>A|p.Leu86Leu |
S251 |
13 | BAS13g01780 | Scaffold13 | 14606217 | G | A | missense_variant | MODERATE | c.568G>A|p.Ala190Thr |
S149 |
14 | BAS13g01780 | Scaffold13 | 14606373 | G | A | missense_variant | MODERATE | c.724G>A|p.Glu242Lys |
S244 |
15 | BAS13g01780 | Scaffold13 | 14608481 | C | T | downstream_gene_variant | MODIFIER | c.*773C>T| |
S48 |