| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 154851 | BAA02g03040 | A02 | 1353601 | C | T | missense_variant | MODERATE | c.869G>A|p.Arg290Lys |
S32 |
| 154852 | BAA02g03040 | A02 | 1355398 | C | T | missense_variant | MODERATE | c.122G>A|p.Gly41Glu |
S99 |
| 154853 | BAA02g03040 | A02 | 1355607 | G | A | upstream_gene_variant | MODIFIER | c.-88C>T| |
S247 |
| 154854 | BAA02g03050 | A02 | 1357103 | G | A | synonymous_variant | LOW | c.811C>T|p.Leu271Leu |
S48 |
| 154855 | BAA02g03050 | A02 | 1357591 | C | T | missense_variant | MODERATE | c.323G>A|p.Ser108Asn |
S257 |
| 154856 | BAA02g03040 | A02 | 1358476 | C | T | upstream_gene_variant | MODIFIER | c.-2957G>A| |
S301 S304 |
| 154857 | BAA02g03040 | A02 | 1358532 | C | T | upstream_gene_variant | MODIFIER | c.-3013G>A| |
S216 |
| 154858 | BAA02g03040 | A02 | 1359559 | G | A | upstream_gene_variant | MODIFIER | c.-4040C>T| |
S203 S55 |
| 154859 | BAA02g03060 | A02 | 1359909 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.113-1G>A| |
S12 |
| 154860 | BAA02g03070 | A02 | 1361249 | C | T | synonymous_variant | LOW | c.798G>A|p.Gln266Gln |
S42 |
| 154861 | BAA02g03070 | A02 | 1361352 | C | T | missense_variant | MODERATE | c.695G>A|p.Gly232Asp |
S142 |
| 154862 | BAA02g03070 | A02 | 1361768 | G | A | synonymous_variant | LOW | c.369C>T|p.Asn123Asn |
S273 |
| 154863 | BAA02g03070 | A02 | 1362202 | G | A | synonymous_variant | LOW | c.33C>T|p.Phe11Phe |
S232 |
| 154864 | BAA02g03070 | A02 | 1363810 | C | T | upstream_gene_variant | MODIFIER | c.-1576G>A| |
S8 |
| 154865 | BAA02g03070 | A02 | 1365168 | C | A | upstream_gene_variant | MODIFIER | c.-2934G>T| |
S206 |
| 154866 | BAA02g03070 | A02 | 1365546 | G | A | upstream_gene_variant | MODIFIER | c.-3312C>T| |
S62 |
| 154867 | BAA02g03070 | A02 | 1366068 | C | T | upstream_gene_variant | MODIFIER | c.-3834G>A| |
S219 |
| 154868 | BAA02g03070 | A02 | 1366112 | C | T | upstream_gene_variant | MODIFIER | c.-3878G>A| |
S159 |
| 154869 | BAA02g03090 | A02 | 1367088 | G | A | missense_variant | MODERATE | c.115G>A|p.Gly39Arg |
S302 |
| 154870 | BAA02g03090 | A02 | 1367555 | C | T | missense_variant | MODERATE | c.347C>T|p.Thr116Ile |
S181 |
| 154871 | BAA02g03090 | A02 | 1367817 | G | A | missense_variant | MODERATE | c.542G>A|p.Gly181Asp |
S59 |
| 154872 | BAA02g03090 | A02 | 1368050 | C | T | missense_variant | MODERATE | c.683C>T|p.Thr228Ile |
S283 |
| 154873 | BAA02g03090 | A02 | 1368267 | C | T | missense_variant | MODERATE | c.820C>T|p.Pro274Ser |
S288 |
| 154874 | BAA02g03080 | A02 | 1369638 | C | T | upstream_gene_variant | MODIFIER | c.-3703G>A| |
S8 |
| 154875 | BAA02g03110 | A02 | 1371209 | G | A | missense_variant | MODERATE | c.242G>A|p.Arg81Lys |
S209 |