Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g20540 | A04 | 23583012 | C | T | upstream_gene_variant | MODIFIER | c.-2896C>T| |
S202 |
2 | BAA04g20540 | A04 | 23584037 | G | T | upstream_gene_variant | MODIFIER | c.-1871G>T| |
S13 |
3 | BAA04g20540 | A04 | 23584465 | G | A | upstream_gene_variant | MODIFIER | c.-1443G>A| |
S298 |
4 | BAA04g20540 | A04 | 23584536 | C | T | upstream_gene_variant | MODIFIER | c.-1372C>T| |
S10 |
5 | BAA04g20540 | A04 | 23584666 | C | T | upstream_gene_variant | MODIFIER | c.-1242C>T| |
S32 |
6 | BAA04g20540 | A04 | 23585363 | C | T | upstream_gene_variant | MODIFIER | c.-545C>T| |
S308 |
7 | BAA04g20540 | A04 | 23585932 | C | T | stop_gained | HIGH | c.25C>T|p.Arg9* |
S138 |
8 | BAA04g20540 | A04 | 23586316 | A | T | missense_variant | MODERATE | c.409A>T|p.Thr137Ser |
S272 |
9 | BAA04g20540 | A04 | 23587031 | C | T | missense_variant | MODERATE | c.1124C>T|p.Pro375Leu |
S140 |
10 | BAA04g20540 | A04 | 23587232 | C | T | missense_variant | MODERATE | c.1325C>T|p.Ser442Phe |
S193 |
11 | BAA04g20540 | A04 | 23587423 | G | A | missense_variant | MODERATE | c.1516G>A|p.Ala506Thr |
S25 |