Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g36520 | A09 | 44816763 | G | A | synonymous_variant | LOW | c.1663C>T|p.Leu555Leu |
S136 |
2 | BAA09g36520 | A09 | 44817140 | G | A | missense_variant | MODERATE | c.1475C>T|p.Ala492Val |
S13 |
3 | BAA09g36520 | A09 | 44817309 | G | A | stop_gained&splice_region_variant | HIGH | c.1381C>T|p.Gln461* |
S305 |
4 | BAA09g36520 | A09 | 44817377 | G | A | missense_variant | MODERATE | c.1313C>T|p.Ala438Val |
S177 |
5 | BAA09g36520 | A09 | 44817484 | C | T | synonymous_variant | LOW | c.1206G>A|p.Arg402Arg |
S50 |
6 | BAA09g36520 | A09 | 44817802 | G | A | synonymous_variant | LOW | c.966C>T|p.Arg322Arg |
S158 |
7 | BAA09g36520 | A09 | 44817972 | G | A | missense_variant | MODERATE | c.796C>T|p.Leu266Phe |
S281 |
8 | BAA09g36520 | A09 | 44819729 | G | A | upstream_gene_variant | MODIFIER | c.-464C>T| |
S16 |
9 | BAA09g36520 | A09 | 44821697 | C | T | upstream_gene_variant | MODIFIER | c.-2432G>A| |
S256 |
10 | BAA09g36520 | A09 | 44821757 | C | T | upstream_gene_variant | MODIFIER | c.-2492G>A| |
S144 |
11 | BAA09g36520 | A09 | 44824227 | C | T | upstream_gene_variant | MODIFIER | c.-4962G>A| |
S43 |