Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g24290 | A02 | 13258818 | C | T | missense_variant | MODERATE | c.1372G>A|p.Gly458Arg |
S270 |
2 | BAA02g24290 | A02 | 13259315 | G | A | missense_variant | MODERATE | c.875C>T|p.Pro292Leu |
S159 S243 |
3 | BAA02g24290 | A02 | 13259408 | G | A | missense_variant | MODERATE | c.782C>T|p.Ala261Val |
S278 |
4 | BAA02g24290 | A02 | 13259715 | G | A | synonymous_variant | LOW | c.564C>T|p.Ile188Ile |
S38 |
5 | BAA02g24290 | A02 | 13259985 | C | T | missense_variant | MODERATE | c.455G>A|p.Gly152Glu |
S46 |
6 | BAA02g24290 | A02 | 13260940 | G | C | upstream_gene_variant | MODIFIER | c.-317C>G| |
S115 S120 S19 S297 S35 S5 |
7 | BAA02g24290 | A02 | 13260993 | G | A | upstream_gene_variant | MODIFIER | c.-370C>T| |
S90 |
8 | BAA02g24290 | A02 | 13261794 | C | T | upstream_gene_variant | MODIFIER | c.-1171G>A| |
S152 |
9 | BAA02g24290 | A02 | 13261811 | C | T | upstream_gene_variant | MODIFIER | c.-1188G>A| |
S8 |
10 | BAA02g24290 | A02 | 13261865 | C | T | upstream_gene_variant | MODIFIER | c.-1242G>A| |
S107 |
11 | BAA02g24290 | A02 | 13262055 | C | T | upstream_gene_variant | MODIFIER | c.-1432G>A| |
S255 |
12 | BAA02g24290 | A02 | 13262237 | G | A | upstream_gene_variant | MODIFIER | c.-1614C>T| |
S228 |
13 | BAA02g24290 | A02 | 13262785 | C | T | upstream_gene_variant | MODIFIER | c.-2162G>A| |
S180 S183 S198 |
14 | BAA02g24290 | A02 | 13264450 | G | A | upstream_gene_variant | MODIFIER | c.-3827C>T| |
S23 |
15 | BAA02g24290 | A02 | 13264647 | C | T | upstream_gene_variant | MODIFIER | c.-4024G>A| |
S183 S198 |