Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g59530 | A09 | 57603017 | G | A | stop_gained | HIGH | c.1447C>T|p.Gln483* |
S143 |
2 | BAA09g59530 | A09 | 57603025 | C | T | missense_variant | MODERATE | c.1439G>A|p.Gly480Glu |
S95 |
3 | BAA09g59530 | A09 | 57603285 | G | A | synonymous_variant | LOW | c.1179C>T|p.Tyr393Tyr |
S79 S84 |
4 | BAA09g59530 | A09 | 57603348 | C | T | synonymous_variant | LOW | c.1116G>A|p.Gln372Gln |
S103 |
5 | BAA09g59530 | A09 | 57603700 | C | T | synonymous_variant | LOW | c.837G>A|p.Lys279Lys |
S81 S85 |
6 | BAA09g59530 | A09 | 57603782 | C | T | missense_variant | MODERATE | c.755G>A|p.Arg252Gln |
S201 |
7 | BAA09g59530 | A09 | 57604460 | C | T | missense_variant | MODERATE | c.169G>A|p.Val57Ile |
S138 |
8 | BAA09g59530 | A09 | 57604988 | G | A | missense_variant | MODERATE | c.56C>T|p.Ser19Phe |
S28 |
9 | BAA09g59530 | A09 | 57605286 | C | T | upstream_gene_variant | MODIFIER | c.-243G>A| |
S230 |
10 | BAA09g59530 | A09 | 57606312 | C | T | upstream_gene_variant | MODIFIER | c.-1269G>A| |
S51 |
11 | BAA09g59530 | A09 | 57606344 | G | A | upstream_gene_variant | MODIFIER | c.-1301C>T| |
S146 |
12 | BAA09g59530 | A09 | 57606731 | C | T | upstream_gene_variant | MODIFIER | c.-1688G>A| |
S256 |
13 | BAA09g59530 | A09 | 57607464 | G | A | upstream_gene_variant | MODIFIER | c.-2421C>T| |
S216 |
14 | BAA09g59530 | A09 | 57607946 | C | T | upstream_gene_variant | MODIFIER | c.-2903G>A| |
S236 |
15 | BAA09g59530 | A09 | 57610029 | G | A | upstream_gene_variant | MODIFIER | c.-4986C>T| |
S148 S210 S30 S31 |