Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g17030 | A06 | 8553350 | C | T | missense_variant | MODERATE | c.916G>A|p.Ala306Thr |
S76 |
2 | BAA06g17030 | A06 | 8553740 | G | A | synonymous_variant | LOW | c.526C>T|p.Leu176Leu |
S88 |
3 | BAA06g17030 | A06 | 8554197 | C | T | synonymous_variant | LOW | c.69G>A|p.Gln23Gln |
S162 |
4 | BAA06g17030 | A06 | 8557139 | C | T | upstream_gene_variant | MODIFIER | c.-2874G>A| |
S176 |
5 | BAA06g17030 | A06 | 8558393 | C | T | upstream_gene_variant | MODIFIER | c.-4128G>A| |
S36 |
6 | BAA06g17030 | A06 | 8558610 | C | T | upstream_gene_variant | MODIFIER | c.-4345G>A| |
S282 |
7 | BAA06g17030 | A06 | 8558624 | C | T | upstream_gene_variant | MODIFIER | c.-4359G>A| |
S94 |