| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 9751 | BAA01g08010 | A01 | 3484011 | C | T | missense_variant | MODERATE | c.415C>T|p.Leu139Phe |
S126 |
| 9752 | BAA01g08020 | A01 | 3485086 | G | A | missense_variant | MODERATE | c.1087C>T|p.Pro363Ser |
S217 |
| 9753 | BAA01g08020 | A01 | 3486033 | C | T | missense_variant | MODERATE | c.415G>A|p.Gly139Arg |
S267 |
| 9754 | BAA01g08020 | A01 | 3486807 | G | A | upstream_gene_variant | MODIFIER | c.-91C>T| |
S306 |
| 9755 | BAA01g08020 | A01 | 3486989 | C | T | upstream_gene_variant | MODIFIER | c.-273G>A| |
S128 |
| 9756 | BAA01g08020 | A01 | 3487929 | C | T | upstream_gene_variant | MODIFIER | c.-1213G>A| |
S231 |
| 9757 | BAA01g08020 | A01 | 3488423 | G | A | upstream_gene_variant | MODIFIER | c.-1707C>T| |
S216 |
| 9758 | BAA01g08020 | A01 | 3488458 | C | T | upstream_gene_variant | MODIFIER | c.-1742G>A| |
S155 |
| 9759 | BAA01g08020 | A01 | 3488796 | C | T | upstream_gene_variant | MODIFIER | c.-2080G>A| |
S19 |
| 9760 | BAA01g08020 | A01 | 3488984 | G | A | upstream_gene_variant | MODIFIER | c.-2268C>T| |
S149 |
| 9761 | BAA01g08020 | A01 | 3490795 | C | T | upstream_gene_variant | MODIFIER | c.-4079G>A| |
S46 |
| 9762 | BAA01g08030 | A01 | 3491100 | C | T | synonymous_variant | LOW | c.33C>T|p.Phe11Phe |
S112 |
| 9763 | BAA01g08030 | A01 | 3491308 | G | A | missense_variant | MODERATE | c.241G>A|p.Ala81Thr |
S5 |
| 9764 | BAA01g08030 | A01 | 3491468 | G | A | missense_variant | MODERATE | c.401G>A|p.Arg134Lys |
S9 |
| 9765 | BAA01g08030 | A01 | 3491722 | G | A | downstream_gene_variant | MODIFIER | c.*112G>A| |
S149 |
| 9766 | BAA01g08030 | A01 | 3493485 | C | T | downstream_gene_variant | MODIFIER | c.*1875C>T| |
S166 |
| 9767 | BAA01g08040 | A01 | 3493914 | C | T | synonymous_variant | LOW | c.1323G>A|p.Leu441Leu |
S148 S30 S31 |
| 9768 | BAA01g08040 | A01 | 3494371 | C | T | missense_variant | MODERATE | c.866G>A|p.Ser289Asn |
S76 |
| 9769 | BAA01g08040 | A01 | 3494872 | G | A | missense_variant | MODERATE | c.365C>T|p.Ser122Phe |
S104 S52 |
| 9770 | BAA01g08040 | A01 | 3496066 | G | A | upstream_gene_variant | MODIFIER | c.-830C>T| |
S251 |
| 9771 | BAA01g08040 | A01 | 3496411 | C | T | upstream_gene_variant | MODIFIER | c.-1175G>A| |
S100 |
| 9772 | BAA01g08040 | A01 | 3499231 | G | A | upstream_gene_variant | MODIFIER | c.-3995C>T| |
S188 |
| 9773 | BAA01g08040 | A01 | 3499947 | G | A | upstream_gene_variant | MODIFIER | c.-4711C>T| |
S238 |
| 9774 | BAA01g08050 | A01 | 3500238 | G | A | upstream_gene_variant | MODIFIER | c.-459C>T| |
S162 |
| 9775 | BAA01g08050 | A01 | 3500915 | G | A | upstream_gene_variant | MODIFIER | c.-1136C>T| |
S188 |