Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g60740 | A03 | 30603543 | G | A | downstream_gene_variant | MODIFIER | c.*423C>T| |
S136 |
2 | BAA03g60740 | A03 | 30604045 | G | A | missense_variant | MODERATE | c.1325C>T|p.Thr442Ile |
S259 |
3 | BAA03g60740 | A03 | 30604376 | T | A | missense_variant | MODERATE | c.1162A>T|p.Ile388Phe |
S79 S84 |
4 | BAA03g60740 | A03 | 30604757 | C | T | intron_variant | MODIFIER | c.996+59G>A| |
S180 |
5 | BAA03g60740 | A03 | 30605247 | G | A | missense_variant | MODERATE | c.676C>T|p.His226Tyr |
S82 S92 |
6 | BAA03g60740 | A03 | 30605321 | G | A | intron_variant | MODIFIER | c.628-26C>T| |
S162 |
7 | BAA03g60740 | A03 | 30605457 | G | A | missense_variant | MODERATE | c.530C>T|p.Ala177Val |
S70 |
8 | BAA03g60740 | A03 | 30605781 | C | T | missense_variant | MODERATE | c.206G>A|p.Gly69Glu |
S187 |
9 | BAA03g60740 | A03 | 30605805 | G | A | missense_variant | MODERATE | c.182C>T|p.Ala61Val |
S268 |
10 | BAA03g60740 | A03 | 30606208 | C | T | upstream_gene_variant | MODIFIER | c.-124G>A| |
S142 |
11 | BAA03g60740 | A03 | 30606878 | C | T | upstream_gene_variant | MODIFIER | c.-794G>A| |
S105 S106 |
12 | BAA03g60740 | A03 | 30608611 | C | T | upstream_gene_variant | MODIFIER | c.-2527G>A| |
S79 S84 |
13 | BAA03g60740 | A03 | 30609784 | G | A | upstream_gene_variant | MODIFIER | c.-3700C>T| |
S109 |
14 | BAA03g60740 | A03 | 30610079 | C | T | upstream_gene_variant | MODIFIER | c.-3995G>A| |
S308 |