| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 81751 | BAA01g43190 | A01 | 28638770 | C | T | upstream_gene_variant | MODIFIER | c.-4726G>A| |
S180 |
| 81752 | BAA01g43210 | A01 | 28640297 | G | A | synonymous_variant | LOW | c.171G>A|p.Leu57Leu |
S292 |
| 81753 | BAA01g43200 | A01 | 28641453 | G | A | upstream_gene_variant | MODIFIER | c.-3499C>T| |
S32 |
| 81754 | BAA01g43210 | A01 | 28641913 | G | A | missense_variant | MODERATE | c.1045G>A|p.Val349Ile |
S303 |
| 81755 | BAA01g43210 | A01 | 28642075 | C | T | missense_variant | MODERATE | c.1207C>T|p.Pro403Ser |
S267 |
| 81756 | BAA01g43210 | A01 | 28642781 | G | A | missense_variant | MODERATE | c.1661G>A|p.Gly554Glu |
S168 |
| 81757 | BAA01g43210 | A01 | 28643283 | C | T | downstream_gene_variant | MODIFIER | c.*237C>T| |
S265 |
| 81758 | BAA01g43210 | A01 | 28643373 | G | A | downstream_gene_variant | MODIFIER | c.*327G>A| |
S273 |
| 81759 | BAA01g43210 | A01 | 28643440 | C | T | downstream_gene_variant | MODIFIER | c.*394C>T| |
S35 |
| 81760 | BAA01g43210 | A01 | 28643790 | C | T | downstream_gene_variant | MODIFIER | c.*744C>T| |
S262 |
| 81761 | BAA01g43220 | A01 | 28644311 | C | T | missense_variant | MODERATE | c.91G>A|p.Glu31Lys |
S181 |
| 81762 | BAA01g43220 | A01 | 28644710 | G | A | upstream_gene_variant | MODIFIER | c.-309C>T| |
S12 |
| 81763 | BAA01g43220 | A01 | 28644711 | G | A | upstream_gene_variant | MODIFIER | c.-310C>T| |
S98 |
| 81764 | BAA01g43220 | A01 | 28645291 | G | A | upstream_gene_variant | MODIFIER | c.-890C>T| |
S48 |
| 81765 | BAA01g43220 | A01 | 28646129 | C | T | upstream_gene_variant | MODIFIER | c.-1728G>A| |
S80 |
| 81766 | BAA01g43220 | A01 | 28648012 | A | T | upstream_gene_variant | MODIFIER | c.-3611T>A| |
S156 |
| 81767 | BAA01g43230 | A01 | 28648592 | C | T | missense_variant | MODERATE | c.2080G>A|p.Ala694Thr |
S34 |
| 81768 | BAA01g43230 | A01 | 28649019 | C | T | synonymous_variant | LOW | c.1653G>A|p.Thr551Thr |
S265 |
| 81769 | BAA01g43230 | A01 | 28649217 | A | C | synonymous_variant | LOW | c.1455T>G|p.Val485Val |
S1 S132 S156 S176 S20 S200 S202 S203 S218 S240 S241 S263 S27 S295 S42 S49 S55 S6 S70 |
| 81770 | BAA01g43230 | A01 | 28650017 | C | T | missense_variant | MODERATE | c.655G>A|p.Asp219Asn |
S217 |
| 81771 | BAA01g43230 | A01 | 28652485 | C | T | upstream_gene_variant | MODIFIER | c.-1814G>A| |
S207 |
| 81772 | BAA01g43240 | A01 | 28652529 | G | A | start_lost | HIGH | c.3G>A|p.Met1? |
S171 |
| 81773 | BAA01g43230 | A01 | 28653684 | T | C | upstream_gene_variant | MODIFIER | c.-3013A>G| |
S33 |
| 81774 | BAA01g43230 | A01 | 28653914 | G | A | upstream_gene_variant | MODIFIER | c.-3243C>T| |
S35 |
| 81775 | BAA01g43230 | A01 | 28655119 | C | T | upstream_gene_variant | MODIFIER | c.-4448G>A| |
S204 |