Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14490 | A02 | 6775023 | G | A | stop_gained | HIGH | c.1615C>T|p.Gln539* |
S187 |
2 | BAA02g14490 | A02 | 6775214 | C | T | missense_variant | MODERATE | c.1424G>A|p.Arg475Lys |
S142 |
3 | BAA02g14490 | A02 | 6776688 | C | T | missense_variant | MODERATE | c.1138G>A|p.Val380Ile |
S88 |
4 | BAA02g14490 | A02 | 6777078 | G | A | stop_gained | HIGH | c.748C>T|p.Arg250* |
S105 S106 |
5 | BAA02g14490 | A02 | 6777105 | G | A | missense_variant | MODERATE | c.721C>T|p.Leu241Phe |
S162 |
6 | BAA02g14490 | A02 | 6777446 | G | A | missense_variant | MODERATE | c.380C>T|p.Ser127Phe |
S157 |
7 | BAA02g14490 | A02 | 6778416 | C | T | upstream_gene_variant | MODIFIER | c.-423G>A| |
S249 |
8 | BAA02g14490 | A02 | 6778505 | C | T | upstream_gene_variant | MODIFIER | c.-512G>A| |
S63 |
9 | BAA02g14490 | A02 | 6778520 | G | A | upstream_gene_variant | MODIFIER | c.-527C>T| |
S125 |
10 | BAA02g14490 | A02 | 6779563 | C | T | upstream_gene_variant | MODIFIER | c.-1570G>A| |
S216 S241 S265 S39 |
11 | BAA02g14490 | A02 | 6780115 | C | T | upstream_gene_variant | MODIFIER | c.-2122G>A| |
S179 |