| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 157151 | BAA02g04930 | A02 | 2151710 | C | T | upstream_gene_variant | MODIFIER | c.-3572C>T| |
S200 |
| 157152 | BAA02g04920 | A02 | 2153101 | C | T | missense_variant | MODERATE | c.14G>A|p.Arg5Lys |
S306 S308 |
| 157153 | BAA02g04920 | A02 | 2153556 | G | A | upstream_gene_variant | MODIFIER | c.-442C>T| |
S162 |
| 157154 | BAA02g04930 | A02 | 2155459 | C | T | missense_variant | MODERATE | c.67C>T|p.Pro23Ser |
S75 S81 |
| 157155 | BAA02g04930 | A02 | 2155500 | G | A | synonymous_variant | LOW | c.108G>A|p.Lys36Lys |
S67 |
| 157156 | BAA02g04930 | A02 | 2157451 | G | A | synonymous_variant | LOW | c.1002G>A|p.Thr334Thr |
S223 |
| 157157 | BAA02g04940 | A02 | 2159641 | C | T | downstream_gene_variant | MODIFIER | c.*2581G>A| |
S47 |
| 157158 | BAA02g04930 | A02 | 2160343 | C | T | missense_variant | MODERATE | c.2818C>T|p.Pro940Ser |
S58 |
| 157159 | BAA02g04930 | A02 | 2160562 | G | A | missense_variant | MODERATE | c.3037G>A|p.Glu1013Lys |
S168 |
| 157160 | BAA02g04930 | A02 | 2160590 | G | A | missense_variant | MODERATE | c.3065G>A|p.Arg1022Lys |
S210 S225 |
| 157161 | BAA02g04930 | A02 | 2161786 | G | A | downstream_gene_variant | MODIFIER | c.*514G>A| |
S215 |
| 157162 | BAA02g04930 | A02 | 2161956 | G | A | downstream_gene_variant | MODIFIER | c.*684G>A| |
S302 |
| 157163 | BAA02g04930 | A02 | 2161983 | C | T | downstream_gene_variant | MODIFIER | c.*711C>T| |
S115 |
| 157164 | BAA02g04930 | A02 | 2162038 | C | T | downstream_gene_variant | MODIFIER | c.*766C>T| |
S18 |
| 157165 | BAA02g04930 | A02 | 2162219 | C | T | downstream_gene_variant | MODIFIER | c.*947C>T| |
S79 S84 |
| 157166 | BAA02g04940 | A02 | 2162266 | C | T | missense_variant | MODERATE | c.1126G>A|p.Ala376Thr |
S13 |
| 157167 | BAA02g04940 | A02 | 2163510 | G | A | missense_variant | MODERATE | c.368C>T|p.Ser123Phe |
S146 |
| 157168 | BAA02g04940 | A02 | 2164500 | C | T | upstream_gene_variant | MODIFIER | c.-66G>A| |
S77 |
| 157169 | BAA02g04940 | A02 | 2164784 | C | T | upstream_gene_variant | MODIFIER | c.-350G>A| |
S138 |
| 157170 | BAA02g04940 | A02 | 2164953 | G | A | upstream_gene_variant | MODIFIER | c.-519C>T| |
S52 |
| 157171 | BAA02g04940 | A02 | 2165380 | C | T | upstream_gene_variant | MODIFIER | c.-946G>A| |
S298 |
| 157172 | BAA02g04940 | A02 | 2165521 | C | T | upstream_gene_variant | MODIFIER | c.-1087G>A| |
S65 |
| 157173 | BAA02g04940 | A02 | 2166566 | C | T | upstream_gene_variant | MODIFIER | c.-2132G>A| |
S117 |
| 157174 | BAA02g04950 | A02 | 2166725 | G | A | synonymous_variant | LOW | c.318C>T|p.Ser106Ser |
S159 |
| 157175 | BAA02g04950 | A02 | 2166746 | C | T | synonymous_variant | LOW | c.297G>A|p.Arg99Arg |
S270 |