| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 5901 | BAA01g04870 | A01 | 2163811 | A | G | synonymous_variant | LOW | c.294T>C|p.Cys98Cys |
S66 |
| 5902 | BAA01g04850 | A01 | 2163969 | C | T | upstream_gene_variant | MODIFIER | c.-4458G>A| |
S210 |
| 5903 | BAA01g04860 | A01 | 2164911 | G | A | upstream_gene_variant | MODIFIER | c.-3299C>T| |
S110 |
| 5904 | BAA01g04860 | A01 | 2165278 | C | T | upstream_gene_variant | MODIFIER | c.-3666G>A| |
S164 |
| 5905 | BAA01g04860 | A01 | 2165426 | C | T | upstream_gene_variant | MODIFIER | c.-3814G>A| |
S8 |
| 5906 | BAA01g04880 | A01 | 2166168 | G | A | missense_variant | MODERATE | c.514G>A|p.Asp172Asn |
S32 |
| 5907 | BAA01g04870 | A01 | 2167527 | G | A | upstream_gene_variant | MODIFIER | c.-2951C>T| |
S293 |
| 5908 | BAA01g04870 | A01 | 2169136 | G | A | upstream_gene_variant | MODIFIER | c.-4560C>T| |
S197 |
| 5909 | BAA01g04890 | A01 | 2170606 | G | A | missense_variant | MODERATE | c.2195C>T|p.Ala732Val |
S196 |
| 5910 | BAA01g04890 | A01 | 2171197 | G | A | missense_variant | MODERATE | c.1817C>T|p.Pro606Leu |
S283 |
| 5911 | BAA01g04890 | A01 | 2172582 | C | T | synonymous_variant | LOW | c.1053G>A|p.Val351Val |
S192 |
| 5912 | BAA01g04890 | A01 | 2172831 | G | A | missense_variant | MODERATE | c.892C>T|p.Leu298Phe |
S180 |
| 5913 | BAA01g04890 | A01 | 2173144 | C | T | missense_variant | MODERATE | c.658G>A|p.Val220Met |
S114 |
| 5914 | BAA01g04880 | A01 | 2173210 | G | A | downstream_gene_variant | MODIFIER | c.*4129G>A| |
S162 |
| 5915 | BAA01g04880 | A01 | 2173222 | G | A | downstream_gene_variant | MODIFIER | c.*4141G>A| |
S83 S88 |
| 5916 | BAA01g04890 | A01 | 2173820 | C | T | missense_variant | MODERATE | c.367G>A|p.Glu123Lys |
S167 |
| 5917 | BAA01g04890 | A01 | 2174069 | G | A | synonymous_variant | LOW | c.118C>T|p.Leu40Leu |
S131 |
| 5918 | BAA01g04900 | A01 | 2175142 | G | A | stop_gained | HIGH | c.1429C>T|p.Gln477* |
S204 |
| 5919 | BAA01g04900 | A01 | 2175306 | G | A | missense_variant | MODERATE | c.1265C>T|p.Ala422Val |
S61 |
| 5920 | BAA01g04900 | A01 | 2175406 | G | A | synonymous_variant | LOW | c.1239C>T|p.Phe413Phe |
S295 |
| 5921 | BAA01g04900 | A01 | 2176302 | C | T | synonymous_variant | LOW | c.639G>A|p.Leu213Leu |
S221 |
| 5922 | BAA01g04900 | A01 | 2177737 | G | A | synonymous_variant | LOW | c.76C>T|p.Leu26Leu |
S161 |
| 5923 | BAA01g04890 | A01 | 2179110 | G | A | upstream_gene_variant | MODIFIER | c.-4924C>T| |
S34 |
| 5924 | BAA01g04900 | A01 | 2179783 | G | A | upstream_gene_variant | MODIFIER | c.-1971C>T| |
S129 |
| 5925 | BAA01g04910 | A01 | 2179957 | G | A | synonymous_variant | LOW | c.93G>A|p.Arg31Arg |
S32 |