| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 157201 | BAA02g04950 | A02 | 2166908 | G | A | missense_variant | MODERATE | c.206C>T|p.Ser69Leu |
S129 |
| 157202 | BAA02g04940 | A02 | 2167202 | G | A | upstream_gene_variant | MODIFIER | c.-2768C>T| |
S308 |
| 157203 | BAA02g04940 | A02 | 2167415 | G | A | upstream_gene_variant | MODIFIER | c.-2981C>T| |
S215 |
| 157204 | BAA02g04940 | A02 | 2167573 | C | T | upstream_gene_variant | MODIFIER | c.-3139G>A| |
S170 |
| 157205 | BAA02g04940 | A02 | 2167581 | G | A | upstream_gene_variant | MODIFIER | c.-3147C>T| |
S188 |
| 157206 | BAA02g04940 | A02 | 2167804 | C | T | upstream_gene_variant | MODIFIER | c.-3370G>A| |
S111 |
| 157207 | BAA02g04960 | A02 | 2168574 | G | A | synonymous_variant | LOW | c.459G>A|p.Glu153Glu |
S36 |
| 157208 | BAA02g04960 | A02 | 2169489 | C | T | splice_region_variant&intron_variant | LOW | c.966-6C>T| |
S79 S84 |
| 157209 | BAA02g04960 | A02 | 2170536 | C | T | missense_variant | MODERATE | c.1486C>T|p.Leu496Phe |
S32 |
| 157210 | BAA02g04970 | A02 | 2172331 | C | T | upstream_gene_variant | MODIFIER | c.-639C>T| |
S37 |
| 157211 | BAA02g04970 | A02 | 2173124 | C | T | missense_variant | MODERATE | c.155C>T|p.Thr52Ile |
S42 |
| 157212 | BAA02g04970 | A02 | 2173169 | G | A | missense_variant | MODERATE | c.200G>A|p.Gly67Asp |
S162 |
| 157213 | BAA02g04980 | A02 | 2175087 | G | A | upstream_gene_variant | MODIFIER | c.-626G>A| |
S23 |
| 157214 | BAA02g05000 | A02 | 2177757 | G | T | upstream_gene_variant | MODIFIER | c.-3301G>T| |
S12 S138 S190 S201 S222 S25 S258 S264 S28 S282 S32 S70 |
| 157215 | BAA02g05000 | A02 | 2178931 | G | A | upstream_gene_variant | MODIFIER | c.-2127G>A| |
S64 |
| 157216 | BAA02g05000 | A02 | 2179143 | G | A | upstream_gene_variant | MODIFIER | c.-1915G>A| |
S34 |
| 157217 | BAA02g05000 | A02 | 2179178 | G | A | upstream_gene_variant | MODIFIER | c.-1880G>A| |
S139 |
| 157218 | BAA02g04990 | A02 | 2181844 | G | A | upstream_gene_variant | MODIFIER | c.-2429C>T| |
S11 |
| 157219 | BAA02g05000 | A02 | 2182540 | G | A | missense_variant | MODERATE | c.553G>A|p.Asp185Asn |
S198 |
| 157220 | BAA02g05000 | A02 | 2182733 | C | T | missense_variant | MODERATE | c.746C>T|p.Ser249Phe |
S201 |
| 157221 | BAA02g05000 | A02 | 2183111 | C | T | missense_variant | MODERATE | c.1022C>T|p.Ala341Val |
S174 |
| 157222 | BAA02g05000 | A02 | 2183221 | G | A | missense_variant | MODERATE | c.1132G>A|p.Gly378Arg |
S153 S213 |
| 157223 | BAA02g05000 | A02 | 2184681 | C | T | downstream_gene_variant | MODIFIER | c.*1236C>T| |
S144 |
| 157224 | BAA02g05010 | A02 | 2185507 | G | A | synonymous_variant | LOW | c.600C>T|p.Tyr200Tyr |
S11 |
| 157225 | BAA02g05000 | A02 | 2185594 | G | A | downstream_gene_variant | MODIFIER | c.*2149G>A| |
S5 |