Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44680 | A09 | 50220568 | G | A | missense_variant | MODERATE | c.1292C>T|p.Ser431Phe |
S176 |
2 | BAA09g44680 | A09 | 50220909 | G | A | synonymous_variant | LOW | c.1053C>T|p.Ala351Ala |
S225 S73 |
3 | BAA09g44680 | A09 | 50221202 | G | A | missense_variant | MODERATE | c.965C>T|p.Ser322Leu |
S281 |
4 | BAA09g44680 | A09 | 50223094 | G | A | synonymous_variant | LOW | c.519C>T|p.Phe173Phe |
S244 |
5 | BAA09g44680 | A09 | 50223828 | C | T | missense_variant | MODERATE | c.34G>A|p.Ala12Thr |
S256 |
6 | BAA09g44680 | A09 | 50224411 | C | T | upstream_gene_variant | MODIFIER | c.-550G>A| |
S30 S31 |
7 | BAA09g44680 | A09 | 50224569 | C | T | upstream_gene_variant | MODIFIER | c.-708G>A| |
S163 |
8 | BAA09g44680 | A09 | 50225471 | G | A | upstream_gene_variant | MODIFIER | c.-1610C>T| |
S172 S217 |
9 | BAA09g44680 | A09 | 50226204 | G | A | upstream_gene_variant | MODIFIER | c.-2343C>T| |
S36 |
10 | BAA09g44680 | A09 | 50226333 | G | A | upstream_gene_variant | MODIFIER | c.-2472C>T| |
S156 |
11 | BAA09g44680 | A09 | 50226457 | G | A | upstream_gene_variant | MODIFIER | c.-2596C>T| |
S81 S85 |
12 | BAA09g44680 | A09 | 50227061 | C | T | upstream_gene_variant | MODIFIER | c.-3200G>A| |
S296 |
13 | BAA09g44680 | A09 | 50228391 | G | T | upstream_gene_variant | MODIFIER | c.-4530C>A| |
S19 S5 |
14 | BAA09g44680 | A09 | 50228527 | G | A | upstream_gene_variant | MODIFIER | c.-4666C>T| |
S88 |