Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03000 | A02 | 1333498 | C | T | synonymous_variant | LOW | c.1188G>A|p.Leu396Leu |
S58 |
2 | BAA02g03000 | A02 | 1333522 | C | T | splice_region_variant&synonymous_variant | LOW | c.1164G>A|p.Gln388Gln |
S181 |
3 | BAA02g03000 | A02 | 1334301 | G | A | synonymous_variant | LOW | c.825C>T|p.Ala275Ala |
S189 |
4 | BAA02g03000 | A02 | 1335407 | G | A | missense_variant | MODERATE | c.544C>T|p.Leu182Phe |
S164 |
5 | BAA02g03000 | A02 | 1336114 | G | A | missense_variant | MODERATE | c.73C>T|p.Leu25Phe |
S208 S93 |
6 | BAA02g03000 | A02 | 1337648 | G | A | upstream_gene_variant | MODIFIER | c.-1462C>T| |
S246 |
7 | BAA02g03000 | A02 | 1337660 | G | A | upstream_gene_variant | MODIFIER | c.-1474C>T| |
S72 |
8 | BAA02g03000 | A02 | 1337710 | G | A | upstream_gene_variant | MODIFIER | c.-1524C>T| |
S134 |
9 | BAA02g03000 | A02 | 1338219 | C | T | upstream_gene_variant | MODIFIER | c.-2033G>A| |
S131 |
10 | BAA02g03000 | A02 | 1338340 | G | A | upstream_gene_variant | MODIFIER | c.-2154C>T| |
S59 |
11 | BAA02g03000 | A02 | 1339402 | G | A | upstream_gene_variant | MODIFIER | c.-3216C>T| |
S165 |