| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 87751 | BAA01g46750 | A01 | 31157625 | C | T | missense_variant | MODERATE | c.118G>A|p.Ala40Thr |
S60 |
| 87752 | BAA01g46750 | A01 | 31157649 | G | A | stop_gained | HIGH | c.94C>T|p.Arg32* |
S5 |
| 87753 | BAA01g46760 | A01 | 31159174 | C | G | missense_variant | MODERATE | c.119C>G|p.Ala40Gly |
S234 |
| 87754 | BAA01g46760 | A01 | 31159685 | C | T | synonymous_variant | LOW | c.630C>T|p.Tyr210Tyr |
S208 S93 |
| 87755 | BAA01g46750 | A01 | 31160051 | G | A | upstream_gene_variant | MODIFIER | c.-2309C>T| |
S36 S71 |
| 87756 | BAA01g46770 | A01 | 31161101 | G | A | stop_gained | HIGH | c.820C>T|p.Gln274* |
S119 |
| 87757 | BAA01g46750 | A01 | 31161184 | G | A | upstream_gene_variant | MODIFIER | c.-3442C>T| |
S95 |
| 87758 | BAA01g46750 | A01 | 31161445 | C | T | upstream_gene_variant | MODIFIER | c.-3703G>A| |
S166 |
| 87759 | BAA01g46770 | A01 | 31162227 | C | T | missense_variant | MODERATE | c.218G>A|p.Arg73His |
S186 |
| 87760 | BAA01g46770 | A01 | 31162986 | G | A | upstream_gene_variant | MODIFIER | c.-542C>T| |
S279 |
| 87761 | BAA01g46780 | A01 | 31163744 | C | T | missense_variant | MODERATE | c.1609G>A|p.Val537Ile |
S260 |
| 87762 | BAA01g46770 | A01 | 31163982 | G | A | upstream_gene_variant | MODIFIER | c.-1538C>T| |
S252 |
| 87763 | BAA01g46770 | A01 | 31164020 | G | A | upstream_gene_variant | MODIFIER | c.-1576C>T| |
S115 |
| 87764 | BAA01g46780 | A01 | 31164331 | G | A | missense_variant | MODERATE | c.1100C>T|p.Pro367Leu |
S276 |
| 87765 | BAA01g46780 | A01 | 31165037 | C | T | missense_variant | MODERATE | c.394G>A|p.Gly132Ser |
S263 |
| 87766 | BAA01g46770 | A01 | 31165434 | G | A | upstream_gene_variant | MODIFIER | c.-2990C>T| |
S295 |
| 87767 | BAA01g46770 | A01 | 31166261 | G | A | upstream_gene_variant | MODIFIER | c.-3817C>T| |
S207 |
| 87768 | BAA01g46770 | A01 | 31166303 | G | A | upstream_gene_variant | MODIFIER | c.-3859C>T| |
S284 |
| 87769 | BAA01g46770 | A01 | 31166319 | G | A | upstream_gene_variant | MODIFIER | c.-3875C>T| |
S123 |
| 87770 | BAA01g46770 | A01 | 31166358 | G | A | upstream_gene_variant | MODIFIER | c.-3914C>T| |
S104 |
| 87771 | BAA01g46770 | A01 | 31166526 | C | T | upstream_gene_variant | MODIFIER | c.-4082G>A| |
S230 |
| 87772 | BAA01g46770 | A01 | 31166663 | G | A | upstream_gene_variant | MODIFIER | c.-4219C>T| |
S196 |
| 87773 | BAA01g46780 | A01 | 31167469 | G | A | upstream_gene_variant | MODIFIER | c.-1856C>T| |
S189 |
| 87774 | BAA01g46780 | A01 | 31167889 | C | T | upstream_gene_variant | MODIFIER | c.-2276G>A| |
S206 S26 |
| 87775 | BAA01g46790 | A01 | 31168632 | C | T | missense_variant | MODERATE | c.517G>A|p.Val173Ile |
S133 |