Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02640 | A02 | 1197762 | G | A | missense_variant | MODERATE | c.4795C>T|p.Pro1599Ser |
S206 S26 |
2 | BAA02g02640 | A02 | 1199598 | G | A | intron_variant | MODIFIER | c.3972+68C>T| |
S163 |
3 | BAA02g02640 | A02 | 1199697 | G | A | missense_variant | MODERATE | c.3941C>T|p.Ser1314Leu |
S188 |
4 | BAA02g02640 | A02 | 1200056 | G | A | missense_variant | MODERATE | c.3667C>T|p.Pro1223Ser |
S264 |
5 | BAA02g02640 | A02 | 1201070 | G | A | missense_variant | MODERATE | c.2653C>T|p.Pro885Ser |
S274 |
6 | BAA02g02640 | A02 | 1201217 | G | A | missense_variant | MODERATE | c.2506C>T|p.Pro836Ser |
S81 S85 |
7 | BAA02g02640 | A02 | 1201289 | G | A | missense_variant | MODERATE | c.2434C>T|p.Pro812Ser |
S61 S98 |
8 | BAA02g02640 | A02 | 1201658 | G | A | missense_variant | MODERATE | c.2065C>T|p.Pro689Ser |
S60 |
9 | BAA02g02640 | A02 | 1202062 | G | A | missense_variant | MODERATE | c.1661C>T|p.Ser554Phe |
S48 |
10 | BAA02g02640 | A02 | 1202161 | C | T | missense_variant | MODERATE | c.1562G>A|p.Gly521Glu |
S272 |
11 | BAA02g02640 | A02 | 1202579 | G | A | missense_variant | MODERATE | c.1144C>T|p.His382Tyr |
S303 |
12 | BAA02g02640 | A02 | 1203819 | G | A | synonymous_variant | LOW | c.390C>T|p.Gly130Gly |
S165 |
13 | BAA02g02640 | A02 | 1207201 | C | T | upstream_gene_variant | MODIFIER | c.-2438G>A| |
S219 |
14 | BAA02g02640 | A02 | 1207230 | G | A | upstream_gene_variant | MODIFIER | c.-2467C>T| |
S171 |
15 | BAA02g02640 | A02 | 1208982 | G | A | upstream_gene_variant | MODIFIER | c.-4219C>T| |
S57 |