| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g33520 | A02 | 28691181 | G | A | missense_variant | MODERATE | c.2909C>T|p.Ala970Val |
S134 |
| 2 | BAA02g33520 | A02 | 28691231 | C | T | synonymous_variant | LOW | c.2859G>A|p.Ser953Ser |
S212 |
| 3 | BAA02g33520 | A02 | 28693299 | C | T | intron_variant | MODIFIER | c.2838-2047G>A| |
S183 S198 |
| 4 | BAA02g33520 | A02 | 28693729 | G | A | intron_variant | MODIFIER | c.2838-2477C>T| |
S196 |
| 5 | BAA02g33520 | A02 | 28693751 | C | T | intron_variant | MODIFIER | c.2838-2499G>A| |
S60 |
| 6 | BAA02g33520 | A02 | 28693884 | G | A | intron_variant | MODIFIER | c.2838-2632C>T| |
S280 |
| 7 | BAA02g33520 | A02 | 28695291 | G | A | intron_variant | MODIFIER | c.2837+2354C>T| |
S269 |
| 8 | BAA02g33520 | A02 | 28695398 | G | A | intron_variant | MODIFIER | c.2837+2247C>T| |
S114 |
| 9 | BAA02g33520 | A02 | 28695628 | G | A | intron_variant | MODIFIER | c.2837+2017C>T| |
S148 S30 S31 |
| 10 | BAA02g33520 | A02 | 28695832 | G | A | intron_variant | MODIFIER | c.2837+1813C>T| |
S291 |
| 11 | BAA02g33520 | A02 | 28695908 | C | T | intron_variant | MODIFIER | c.2837+1737G>A| |
S308 |
| 12 | BAA02g33520 | A02 | 28695926 | G | A | intron_variant | MODIFIER | c.2837+1719C>T| |
S95 |
| 13 | BAA02g33520 | A02 | 28696046 | C | T | intron_variant | MODIFIER | c.2837+1599G>A| |
S15 S3 |
| 14 | BAA02g33520 | A02 | 28696183 | C | T | intron_variant | MODIFIER | c.2837+1462G>A| |
S79 S91 |
| 15 | BAA02g33520 | A02 | 28696597 | C | T | intron_variant | MODIFIER | c.2837+1048G>A| |
S112 |
| 16 | BAA02g33520 | A02 | 28697694 | G | A | synonymous_variant | LOW | c.2788C>T|p.Leu930Leu |
S161 |
| 17 | BAA02g33520 | A02 | 28698445 | G | A | synonymous_variant | LOW | c.2037C>T|p.Asn679Asn |
S71 |
| 18 | BAA02g33520 | A02 | 28698577 | G | A | synonymous_variant | LOW | c.1905C>T|p.Ile635Ile |
S291 |
| 19 | BAA02g33520 | A02 | 28699128 | G | A | splice_region_variant&intron_variant | LOW | c.1705+5C>T| |
S228 |
| 20 | BAA02g33520 | A02 | 28699282 | G | A | missense_variant | MODERATE | c.1556C>T|p.Ser519Phe |
S129 |
| 21 | BAA02g33520 | A02 | 28699439 | C | T | missense_variant | MODERATE | c.1399G>A|p.Glu467Lys |
S2 S4 S6 |
| 22 | BAA02g33520 | A02 | 28699595 | G | A | missense_variant | MODERATE | c.1243C>T|p.Pro415Ser |
S136 |
| 23 | BAA02g33520 | A02 | 28700536 | G | A | missense_variant | MODERATE | c.302C>T|p.Thr101Ile |
S5 |
| 24 | BAA02g33520 | A02 | 28700820 | G | A | synonymous_variant | LOW | c.18C>T|p.Leu6Leu |
S298 |
| 25 | BAA02g33520 | A02 | 28701587 | C | T | upstream_gene_variant | MODIFIER | c.-750G>A| |
S53 |