Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02470 | A02 | 1102283 | G | A | upstream_gene_variant | MODIFIER | c.-1404G>A| |
S286 |
2 | BAA02g02470 | A02 | 1103197 | C | T | upstream_gene_variant | MODIFIER | c.-490C>T| |
S193 |
3 | BAA02g02470 | A02 | 1103810 | G | A | missense_variant | MODERATE | c.124G>A|p.Ala42Thr |
S163 |
4 | BAA02g02470 | A02 | 1104251 | C | T | missense_variant | MODERATE | c.449C>T|p.Ala150Val |
S252 |
5 | BAA02g02470 | A02 | 1104275 | G | A | missense_variant | MODERATE | c.473G>A|p.Ser158Asn |
S225 S73 |
6 | BAA02g02470 | A02 | 1104284 | C | T | missense_variant | MODERATE | c.482C>T|p.Thr161Ile |
S81 S85 |
7 | BAA02g02470 | A02 | 1104485 | C | T | missense_variant | MODERATE | c.683C>T|p.Ser228Leu |
S249 |
8 | BAA02g02470 | A02 | 1104493 | G | A | missense_variant | MODERATE | c.691G>A|p.Gly231Ser |
S15 S2 S3 S34 |
9 | BAA02g02470 | A02 | 1105055 | C | T | downstream_gene_variant | MODIFIER | c.*485C>T| |
S221 |
10 | BAA02g02470 | A02 | 1106369 | C | T | downstream_gene_variant | MODIFIER | c.*1799C>T| |
S240 |
11 | BAA02g02470 | A02 | 1107240 | C | T | downstream_gene_variant | MODIFIER | c.*2670C>T| |
S100 |
12 | BAA02g02470 | A02 | 1107880 | C | T | downstream_gene_variant | MODIFIER | c.*3310C>T| |
S37 |
13 | BAA02g02470 | A02 | 1108390 | G | A | downstream_gene_variant | MODIFIER | c.*3820G>A| |
S51 |