| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 153001 | BAA02g01480 | A02 | 681754 | G | A | upstream_gene_variant | MODIFIER | c.-3598C>T| |
S23 |
| 153002 | BAA02g01490 | A02 | 682767 | C | T | missense_variant | MODERATE | c.1009G>A|p.Glu337Lys |
S70 |
| 153003 | BAA02g01490 | A02 | 682817 | G | A | missense_variant | MODERATE | c.959C>T|p.Ala320Val |
S276 |
| 153004 | BAA02g01490 | A02 | 683758 | G | A | missense_variant | MODERATE | c.638C>T|p.Ser213Leu |
S265 |
| 153005 | BAA02g01490 | A02 | 684636 | C | T | synonymous_variant | LOW | c.246G>A|p.Leu82Leu |
S292 |
| 153006 | BAA02g01500 | A02 | 686603 | G | A | missense_variant | MODERATE | c.1559C>T|p.Ser520Phe |
S183 S198 |
| 153007 | BAA02g01500 | A02 | 686882 | C | T | missense_variant | MODERATE | c.1280G>A|p.Gly427Asp |
S262 |
| 153008 | BAA02g01500 | A02 | 687014 | G | A | missense_variant | MODERATE | c.1148C>T|p.Thr383Ile |
S291 |
| 153009 | BAA02g01500 | A02 | 687617 | C | T | missense_variant | MODERATE | c.545G>A|p.Arg182Lys |
S284 |
| 153010 | BAA02g01490 | A02 | 688279 | G | A | upstream_gene_variant | MODIFIER | c.-3186C>T| |
S44 |
| 153011 | BAA02g01510 | A02 | 689269 | G | A | missense_variant | MODERATE | c.65G>A|p.Arg22Lys |
S210 |
| 153012 | BAA02g01490 | A02 | 689474 | G | A | upstream_gene_variant | MODIFIER | c.-4381C>T| |
S173 |
| 153013 | BAA02g01510 | A02 | 690290 | G | A | missense_variant | MODERATE | c.227G>A|p.Arg76Lys |
S297 |
| 153014 | BAA02g01510 | A02 | 690369 | G | A | synonymous_variant | LOW | c.306G>A|p.Arg102Arg |
S206 S26 |
| 153015 | BAA02g01500 | A02 | 691133 | G | A | upstream_gene_variant | MODIFIER | c.-2972C>T| |
S98 |
| 153016 | BAA02g01500 | A02 | 691252 | C | T | upstream_gene_variant | MODIFIER | c.-3091G>A| |
S181 |
| 153017 | BAA02g01520 | A02 | 692072 | G | A | synonymous_variant | LOW | c.255G>A|p.Lys85Lys |
S20 |
| 153018 | BAA02g01520 | A02 | 692361 | G | A | missense_variant | MODERATE | c.352G>A|p.Ala118Thr |
S44 |
| 153019 | BAA02g01520 | A02 | 693074 | G | A | missense_variant | MODERATE | c.560G>A|p.Arg187Lys |
S263 |
| 153020 | BAA02g01520 | A02 | 693248 | C | T | missense_variant | MODERATE | c.631C>T|p.Pro211Ser |
S92 |
| 153021 | BAA02g01530 | A02 | 694191 | G | A | missense_variant | MODERATE | c.1612C>T|p.Pro538Ser |
S87 |
| 153022 | BAA02g01530 | A02 | 694263 | C | T | missense_variant | MODERATE | c.1540G>A|p.Glu514Lys |
S242 |
| 153023 | BAA02g01530 | A02 | 696415 | G | A | upstream_gene_variant | MODIFIER | c.-245C>T| |
S221 |
| 153024 | BAA02g01530 | A02 | 697859 | C | T | upstream_gene_variant | MODIFIER | c.-1689G>A| |
S179 S278 |
| 153025 | BAA02g01530 | A02 | 698043 | G | A | upstream_gene_variant | MODIFIER | c.-1873C>T| |
S114 |