| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g36150 | A02 | 31036059 | G | A | upstream_gene_variant | MODIFIER | c.-290G>A| |
S133 |
| 2 | BAA02g36150 | A02 | 31037099 | C | T | missense_variant | MODERATE | c.104C>T|p.Ser35Phe |
S170 |
| 3 | BAA02g36150 | A02 | 31037954 | G | A | missense_variant | MODERATE | c.610G>A|p.Ala204Thr |
S113 |
| 4 | BAA02g36150 | A02 | 31038948 | C | T | missense_variant | MODERATE | c.1285C>T|p.Pro429Ser |
S170 |
| 5 | BAA02g36150 | A02 | 31039377 | C | T | splice_region_variant&intron_variant | LOW | c.1524+7C>T| |
S33 |
| 6 | BAA02g36150 | A02 | 31040273 | C | T | intron_variant | MODIFIER | c.2055-26C>T| |
S182 |
| 7 | BAA02g36150 | A02 | 31040586 | C | T | missense_variant | MODERATE | c.2263C>T|p.Pro755Ser |
S98 |
| 8 | BAA02g36150 | A02 | 31040697 | C | T | intron_variant | MODIFIER | c.2331+43C>T| |
S189 |
| 9 | BAA02g36150 | A02 | 31041016 | G | A | missense_variant | MODERATE | c.2473G>A|p.Gly825Arg |
S25 |
| 10 | BAA02g36150 | A02 | 31042001 | G | A | missense_variant | MODERATE | c.3106G>A|p.Asp1036Asn |
S168 |
| 11 | BAA02g36150 | A02 | 31042279 | C | T | missense_variant | MODERATE | c.3230C>T|p.Pro1077Leu |
S208 S93 |
| 12 | BAA02g36150 | A02 | 31042997 | C | T | missense_variant | MODERATE | c.3710C>T|p.Pro1237Leu |
S87 |
| 13 | BAA02g36150 | A02 | 31043323 | C | T | missense_variant | MODERATE | c.3953C>T|p.Ser1318Phe |
S194 S33 |
| 14 | BAA02g36150 | A02 | 31043770 | G | A | missense_variant | MODERATE | c.4099G>A|p.Val1367Ile |
S236 |
| 15 | BAA02g36150 | A02 | 31044803 | G | A | synonymous_variant | LOW | c.4536G>A|p.Lys1512Lys |
S103 |
| 16 | BAA02g36150 | A02 | 31044918 | C | T | missense_variant | MODERATE | c.4651C>T|p.Pro1551Ser |
S97 |
| 17 | BAA02g36150 | A02 | 31048306 | C | T | downstream_gene_variant | MODIFIER | c.*3099C>T| |
S139 S84 S93 |
| 18 | BAA02g36150 | A02 | 31049634 | G | A | downstream_gene_variant | MODIFIER | c.*4427G>A| |
S291 |
| 19 | BAA02g36150 | A02 | 31050094 | G | A | downstream_gene_variant | MODIFIER | c.*4887G>A| |
S238 |
| 20 | BAA02g36150 | A02 | 31050109 | G | A | downstream_gene_variant | MODIFIER | c.*4902G>A| |
S293 |