| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 33151 | BAA01g22630 | A01 | 11439805 | G | A | upstream_gene_variant | MODIFIER | c.-2004G>A| |
S105 S106 |
| 33152 | BAA01g22630 | A01 | 11440052 | C | T | upstream_gene_variant | MODIFIER | c.-1757C>T| |
S176 |
| 33153 | BAA01g22630 | A01 | 11441061 | G | A | upstream_gene_variant | MODIFIER | c.-748G>A| |
S74 |
| 33154 | BAA01g22630 | A01 | 11441302 | C | T | upstream_gene_variant | MODIFIER | c.-507C>T| |
S44 |
| 33155 | BAA01g22630 | A01 | 11441856 | C | T | synonymous_variant | LOW | c.48C>T|p.Ser16Ser |
S47 |
| 33156 | BAA01g22640 | A01 | 11442586 | G | A | upstream_gene_variant | MODIFIER | c.-3144G>A| |
S280 |
| 33157 | BAA01g22640 | A01 | 11443746 | A | G | upstream_gene_variant | MODIFIER | c.-1984A>G| |
S138 |
| 33158 | BAA01g22640 | A01 | 11443927 | T | C | upstream_gene_variant | MODIFIER | c.-1803T>C| |
S28 |
| 33159 | BAA01g22640 | A01 | 11444941 | C | T | upstream_gene_variant | MODIFIER | c.-789C>T| |
S171 |
| 33160 | BAA01g22640 | A01 | 11445903 | G | A | synonymous_variant | LOW | c.174G>A|p.Lys58Lys |
S251 |
| 33161 | BAA01g22630 | A01 | 11446000 | G | A | downstream_gene_variant | MODIFIER | c.*2398G>A| |
S45 |
| 33162 | BAA01g22630 | A01 | 11446452 | C | T | downstream_gene_variant | MODIFIER | c.*2850C>T| |
S286 |
| 33163 | BAA01g22630 | A01 | 11446724 | G | A | downstream_gene_variant | MODIFIER | c.*3122G>A| |
S298 |
| 33164 | BAA01g22630 | A01 | 11447972 | G | A | downstream_gene_variant | MODIFIER | c.*4370G>A| |
S306 S308 |
| 33165 | BAA01g22640 | A01 | 11448672 | C | T | synonymous_variant | LOW | c.574C>T|p.Leu192Leu |
S103 |
| 33166 | BAA01g22640 | A01 | 11448723 | G | A | missense_variant | MODERATE | c.625G>A|p.Gly209Arg |
S299 |
| 33167 | BAA01g22650 | A01 | 11448822 | C | T | downstream_gene_variant | MODIFIER | c.*3840G>A| |
S185 |
| 33168 | BAA01g22640 | A01 | 11451011 | C | T | synonymous_variant | LOW | c.2250C>T|p.Arg750Arg |
S176 |
| 33169 | BAA01g22640 | A01 | 11451526 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2518-1G>A| |
S197 |
| 33170 | BAA01g22650 | A01 | 11452044 | C | T | downstream_gene_variant | MODIFIER | c.*618G>A| |
S210 S225 |
| 33171 | BAA01g22650 | A01 | 11453081 | G | A | missense_variant | MODERATE | c.395C>T|p.Ser132Phe |
S288 |
| 33172 | BAA01g22650 | A01 | 11453139 | C | T | missense_variant | MODERATE | c.337G>A|p.Glu113Lys |
S264 |
| 33173 | BAA01g22640 | A01 | 11453770 | C | T | downstream_gene_variant | MODIFIER | c.*1636C>T| |
S210 S225 |
| 33174 | BAA01g22660 | A01 | 11454791 | G | A | synonymous_variant | LOW | c.751C>T|p.Leu251Leu |
S126 |
| 33175 | BAA01g22660 | A01 | 11454878 | C | T | missense_variant | MODERATE | c.664G>A|p.Glu222Lys |
S179 |