Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26690 | A05 | 31284356 | G | A | intron_variant | MODIFIER | c.1861-180C>T| |
S203 |
2 | BAA05g26690 | A05 | 31284507 | C | T | intron_variant | MODIFIER | c.1861-331G>A| |
S207 |
3 | BAA05g26690 | A05 | 31286565 | G | A | missense_variant | MODERATE | c.1322C>T|p.Pro441Leu |
S216 S265 |
4 | BAA05g26690 | A05 | 31288929 | C | T | upstream_gene_variant | MODIFIER | c.-383G>A| |
S189 |
5 | BAA05g26690 | A05 | 31290361 | C | T | upstream_gene_variant | MODIFIER | c.-1815G>A| |
S183 S198 |
6 | BAA05g26690 | A05 | 31290685 | C | T | upstream_gene_variant | MODIFIER | c.-2139G>A| |
S108 |
7 | BAA05g26690 | A05 | 31291152 | C | T | upstream_gene_variant | MODIFIER | c.-2606G>A| |
S244 |
8 | BAA05g26690 | A05 | 31291458 | G | A | upstream_gene_variant | MODIFIER | c.-2912C>T| |
S25 |
9 | BAA05g26690 | A05 | 31291502 | C | T | upstream_gene_variant | MODIFIER | c.-2956G>A| |
S170 |
10 | BAA05g26690 | A05 | 31293266 | C | T | upstream_gene_variant | MODIFIER | c.-4720G>A| |
S84 S93 |