| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 218951 | BAA02g33060 | A02 | 28328179 | G | A | upstream_gene_variant | MODIFIER | c.-3147C>T| |
S136 |
| 218952 | BAA02g33060 | A02 | 28328337 | C | T | upstream_gene_variant | MODIFIER | c.-3305G>A| |
S116 |
| 218953 | BAA02g33060 | A02 | 28328431 | G | T | upstream_gene_variant | MODIFIER | c.-3399C>A| |
S168 |
| 218954 | BAA02g33060 | A02 | 28329394 | A | G | upstream_gene_variant | MODIFIER | c.-4362T>C| |
S183 S198 |
| 218955 | BAA02g33070 | A02 | 28329667 | G | A | missense_variant | MODERATE | c.296G>A|p.Arg99Lys |
S256 |
| 218956 | BAA02g33070 | A02 | 28329682 | G | A | missense_variant | MODERATE | c.311G>A|p.Gly104Glu |
S155 S211 |
| 218957 | BAA02g33070 | A02 | 28330866 | C | T | intron_variant | MODIFIER | c.692-27C>T| |
S296 |
| 218958 | BAA02g33070 | A02 | 28331781 | C | T | downstream_gene_variant | MODIFIER | c.*471C>T| |
S281 |
| 218959 | BAA02g33070 | A02 | 28332061 | G | A | downstream_gene_variant | MODIFIER | c.*751G>A| |
S301 S304 |
| 218960 | BAA02g33080 | A02 | 28335358 | G | A | upstream_gene_variant | MODIFIER | c.-1721G>A| |
S272 |
| 218961 | BAA02g33080 | A02 | 28335948 | C | T | upstream_gene_variant | MODIFIER | c.-1131C>T| |
S112 |
| 218962 | BAA02g33080 | A02 | 28337003 | G | A | upstream_gene_variant | MODIFIER | c.-76G>A| |
S8 |
| 218963 | BAA02g33090 | A02 | 28338645 | G | A | synonymous_variant | LOW | c.672G>A|p.Lys224Lys |
S267 |
| 218964 | BAA02g33090 | A02 | 28338757 | G | A | missense_variant | MODERATE | c.784G>A|p.Asp262Asn |
S200 |
| 218965 | BAA02g33090 | A02 | 28338772 | G | A | missense_variant | MODERATE | c.799G>A|p.Asp267Asn |
S129 |
| 218966 | BAA02g33090 | A02 | 28339399 | G | A | missense_variant | MODERATE | c.1426G>A|p.Ala476Thr |
S136 |
| 218967 | BAA02g33090 | A02 | 28339566 | G | A | synonymous_variant | LOW | c.1593G>A|p.Lys531Lys |
S238 |
| 218968 | BAA02g33080 | A02 | 28339948 | G | A | downstream_gene_variant | MODIFIER | c.*2549G>A| |
S45 |
| 218969 | BAA02g33090 | A02 | 28340040 | C | T | missense_variant | MODERATE | c.1771C>T|p.Pro591Ser |
S216 |
| 218970 | BAA02g33080 | A02 | 28340113 | G | A | downstream_gene_variant | MODIFIER | c.*2714G>A| |
S155 S211 |
| 218971 | BAA02g33080 | A02 | 28340261 | G | A | downstream_gene_variant | MODIFIER | c.*2862G>A| |
S266 |
| 218972 | BAA02g33080 | A02 | 28340589 | G | A | downstream_gene_variant | MODIFIER | c.*3190G>A| |
S81 S85 |
| 218973 | BAA02g33080 | A02 | 28340791 | C | T | downstream_gene_variant | MODIFIER | c.*3392C>T| |
S212 |
| 218974 | BAA02g33080 | A02 | 28340794 | G | A | downstream_gene_variant | MODIFIER | c.*3395G>A| |
S187 |
| 218975 | BAA02g33080 | A02 | 28340848 | G | A | downstream_gene_variant | MODIFIER | c.*3449G>A| |
S238 |