Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46560 | A02 | 37813439 | G | A | missense_variant | MODERATE | c.130G>A|p.Gly44Arg |
S229 |
2 | BAA02g46560 | A02 | 37814233 | G | A | intron_variant | MODIFIER | c.466-89G>A| |
S142 |
3 | BAA02g46560 | A02 | 37814429 | G | A | stop_gained | HIGH | c.573G>A|p.Trp191* |
S10 |
4 | BAA02g46560 | A02 | 37814631 | G | A | stop_gained | HIGH | c.696G>A|p.Trp232* |
S292 |
5 | BAA02g46560 | A02 | 37814685 | C | T | intron_variant | MODIFIER | c.705-35C>T| |
S90 |
6 | BAA02g46560 | A02 | 37815484 | G | A | missense_variant | MODERATE | c.1136G>A|p.Gly379Asp |
S157 S163 |
7 | BAA02g46560 | A02 | 37816702 | C | T | missense_variant | MODERATE | c.1825C>T|p.Leu609Phe |
S13 |
8 | BAA02g46560 | A02 | 37817273 | G | A | downstream_gene_variant | MODIFIER | c.*235G>A| |
S291 |
9 | BAA02g46560 | A02 | 37820188 | C | T | downstream_gene_variant | MODIFIER | c.*3150C>T| |
S192 |
10 | BAA02g46560 | A02 | 37821166 | A | T | downstream_gene_variant | MODIFIER | c.*4128A>T| |
S50 |