Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g31540 | A02 | 18954172 | G | A | synonymous_variant | LOW | c.2160C>T|p.Ile720Ile |
S80 |
2 | BAA02g31540 | A02 | 18954684 | G | A | synonymous_variant | LOW | c.1648C>T|p.Leu550Leu |
S20 |
3 | BAA02g31540 | A02 | 18954740 | G | A | missense_variant | MODERATE | c.1592C>T|p.Ser531Phe |
S4 |
4 | BAA02g31540 | A02 | 18955086 | G | A | splice_region_variant&intron_variant | LOW | c.1478+5C>T| |
S62 |
5 | BAA02g31540 | A02 | 18956213 | G | A | missense_variant | MODERATE | c.533C>T|p.Pro178Leu |
S246 |
6 | BAA02g31540 | A02 | 18956343 | G | A | missense_variant | MODERATE | c.403C>T|p.Pro135Ser |
S148 S30 S31 S80 |
7 | BAA02g31540 | A02 | 18956355 | G | A | missense_variant&splice_region_variant | MODERATE | c.391C>T|p.Leu131Phe |
S249 |
8 | BAA02g31540 | A02 | 18958614 | G | A | intron_variant | MODIFIER | c.212+835C>T| |
S286 |
9 | BAA02g31540 | A02 | 18958893 | C | T | intron_variant | MODIFIER | c.212+556G>A| |
S216 |
10 | BAA02g31540 | A02 | 18959276 | G | A | intron_variant | MODIFIER | c.212+173C>T| |
S229 |
11 | BAA02g31540 | A02 | 18960341 | C | T | upstream_gene_variant | MODIFIER | c.-681G>A| |
S299 |