Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26700 | A05 | 31295003 | G | A | upstream_gene_variant | MODIFIER | c.-4671G>A| |
S217 S248 |
2 | BAA05g26700 | A05 | 31295185 | G | A | upstream_gene_variant | MODIFIER | c.-4489G>A| |
S82 S92 |
3 | BAA05g26700 | A05 | 31295417 | G | A | upstream_gene_variant | MODIFIER | c.-4257G>A| |
S41 |
4 | BAA05g26700 | A05 | 31295556 | G | A | upstream_gene_variant | MODIFIER | c.-4118G>A| |
S136 |
5 | BAA05g26700 | A05 | 31296078 | G | A | upstream_gene_variant | MODIFIER | c.-3596G>A| |
S200 |
6 | BAA05g26700 | A05 | 31296489 | G | A | upstream_gene_variant | MODIFIER | c.-3185G>A| |
S283 |
7 | BAA05g26700 | A05 | 31296986 | G | A | upstream_gene_variant | MODIFIER | c.-2688G>A| |
S281 |
8 | BAA05g26700 | A05 | 31298012 | C | T | upstream_gene_variant | MODIFIER | c.-1662C>T| |
S206 S26 |
9 | BAA05g26700 | A05 | 31299718 | C | T | synonymous_variant | LOW | c.45C>T|p.Tyr15Tyr |
S208 S219 |
10 | BAA05g26700 | A05 | 31299787 | C | T | synonymous_variant | LOW | c.114C>T|p.Asp38Asp |
S288 |
11 | BAA05g26700 | A05 | 31303467 | G | A | missense_variant | MODERATE | c.1589G>A|p.Gly530Glu |
S205 |
12 | BAA05g26700 | A05 | 31303611 | C | T | missense_variant | MODERATE | c.1733C>T|p.Pro578Leu |
S13 |