Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g16290 | A06 | 8094106 | C | T | missense_variant | MODERATE | c.1591G>A|p.Val531Ile |
S212 |
2 | BAA06g16290 | A06 | 8094439 | C | T | stop_gained | HIGH | c.1322G>A|p.Trp441* |
S87 |
3 | BAA06g16290 | A06 | 8095334 | C | T | synonymous_variant | LOW | c.849G>A|p.Thr283Thr |
S56 |
4 | BAA06g16290 | A06 | 8095359 | G | A | missense_variant | MODERATE | c.824C>T|p.Pro275Leu |
S273 |
5 | BAA06g16290 | A06 | 8095536 | C | T | synonymous_variant | LOW | c.741G>A|p.Arg247Arg |
S162 |
6 | BAA06g16290 | A06 | 8096129 | G | A | splice_region_variant&intron_variant | LOW | c.344+3C>T| |
S136 |
7 | BAA06g16290 | A06 | 8097487 | C | T | upstream_gene_variant | MODIFIER | c.-850G>A| |
S77 S82 |
8 | BAA06g16290 | A06 | 8097594 | C | T | upstream_gene_variant | MODIFIER | c.-957G>A| |
S189 |
9 | BAA06g16290 | A06 | 8098695 | G | A | upstream_gene_variant | MODIFIER | c.-2058C>T| |
S5 |