Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02240 | A02 | 1005238 | G | A | upstream_gene_variant | MODIFIER | c.-4621G>A| |
S153 S213 |
2 | BAA02g02240 | A02 | 1005981 | G | A | upstream_gene_variant | MODIFIER | c.-3878G>A| |
S149 |
3 | BAA02g02240 | A02 | 1005996 | G | A | upstream_gene_variant | MODIFIER | c.-3863G>A| |
S241 |
4 | BAA02g02240 | A02 | 1009932 | C | T | missense_variant | MODERATE | c.74C>T|p.Pro25Leu |
S230 |
5 | BAA02g02240 | A02 | 1010055 | C | T | missense_variant | MODERATE | c.197C>T|p.Ser66Phe |
S179 |
6 | BAA02g02240 | A02 | 1010225 | C | T | synonymous_variant | LOW | c.367C>T|p.Leu123Leu |
S65 |
7 | BAA02g02240 | A02 | 1010336 | G | A | missense_variant | MODERATE | c.478G>A|p.Glu160Lys |
S188 |
8 | BAA02g02240 | A02 | 1010586 | G | A | missense_variant | MODERATE | c.728G>A|p.Gly243Asp |
S203 |
9 | BAA02g02240 | A02 | 1010678 | C | T | missense_variant | MODERATE | c.820C>T|p.Pro274Ser |
S71 |
10 | BAA02g02240 | A02 | 1010927 | G | A | missense_variant | MODERATE | c.1069G>A|p.Val357Met |
S279 |
11 | BAA02g02240 | A02 | 1011911 | C | T | missense_variant | MODERATE | c.2053C>T|p.His685Tyr |
S117 |
12 | BAA02g02240 | A02 | 1012347 | C | T | synonymous_variant | LOW | c.2421C>T|p.Phe807Phe |
S18 |
13 | BAA02g02240 | A02 | 1017069 | T | G | downstream_gene_variant | MODIFIER | c.*4662T>G| |
S18 |
14 | BAA02g02240 | A02 | 1017123 | G | A | downstream_gene_variant | MODIFIER | c.*4716G>A| |
S172 S202 S217 |
15 | BAA02g02240 | A02 | 1017125 | G | A | downstream_gene_variant | MODIFIER | c.*4718G>A| |
S11 |
16 | BAA02g02240 | A02 | 1017292 | C | T | downstream_gene_variant | MODIFIER | c.*4885C>T| |
S245 |