| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 157601 | BAA02g05270 | A02 | 2308501 | C | T | synonymous_variant | LOW | c.207G>A|p.Thr69Thr |
S42 |
| 157602 | BAA02g05270 | A02 | 2308513 | A | G | synonymous_variant | LOW | c.195T>C|p.Ala65Ala |
S268 |
| 157603 | BAA02g05270 | A02 | 2308844 | G | A | upstream_gene_variant | MODIFIER | c.-47C>T| |
S17 |
| 157604 | BAA02g05270 | A02 | 2309111 | C | T | upstream_gene_variant | MODIFIER | c.-314G>A| |
S97 |
| 157605 | BAA02g05270 | A02 | 2309885 | C | T | upstream_gene_variant | MODIFIER | c.-1088G>A| |
S65 |
| 157606 | BAA02g05280 | A02 | 2310196 | C | T | missense_variant | MODERATE | c.275C>T|p.Ala92Val |
S135 |
| 157607 | BAA02g05280 | A02 | 2310689 | G | A | missense_variant | MODERATE | c.692G>A|p.Gly231Asp |
S189 |
| 157608 | BAA02g05280 | A02 | 2310715 | C | T | missense_variant | MODERATE | c.718C>T|p.Leu240Phe |
S16 |
| 157609 | BAA02g05280 | A02 | 2311005 | C | T | missense_variant | MODERATE | c.914C>T|p.Pro305Leu |
S219 |
| 157610 | BAA02g05280 | A02 | 2311012 | C | T | synonymous_variant | LOW | c.921C>T|p.Asp307Asp |
S116 |
| 157611 | BAA02g05280 | A02 | 2311068 | C | T | missense_variant | MODERATE | c.977C>T|p.Ser326Phe |
S38 |
| 157612 | BAA02g05280 | A02 | 2311210 | G | A | synonymous_variant | LOW | c.1119G>A|p.Lys373Lys |
S265 |
| 157613 | BAA02g05270 | A02 | 2311617 | C | A | upstream_gene_variant | MODIFIER | c.-2820G>T| |
S198 S213 |
| 157614 | BAA02g05270 | A02 | 2312027 | G | A | upstream_gene_variant | MODIFIER | c.-3230C>T| |
S266 |
| 157615 | BAA02g05270 | A02 | 2312780 | C | T | upstream_gene_variant | MODIFIER | c.-3983G>A| |
S28 |
| 157616 | BAA02g05290 | A02 | 2314397 | G | A | missense_variant | MODERATE | c.325G>A|p.Glu109Lys |
S238 |
| 157617 | BAA02g05290 | A02 | 2314451 | G | A | missense_variant | MODERATE | c.379G>A|p.Asp127Asn |
S302 |
| 157618 | BAA02g05300 | A02 | 2314852 | C | T | synonymous_variant | LOW | c.1830G>A|p.Lys610Lys |
S187 |
| 157619 | BAA02g05300 | A02 | 2315704 | G | A | synonymous_variant | LOW | c.1191C>T|p.Phe397Phe |
S126 |
| 157620 | BAA02g05280 | A02 | 2316158 | G | A | downstream_gene_variant | MODIFIER | c.*2615G>A| |
S170 |
| 157621 | BAA02g05280 | A02 | 2316206 | C | T | downstream_gene_variant | MODIFIER | c.*2663C>T| |
S138 |
| 157622 | BAA02g05300 | A02 | 2316960 | C | T | missense_variant | MODERATE | c.512G>A|p.Arg171Gln |
S8 |
| 157623 | BAA02g05300 | A02 | 2317164 | G | A | missense_variant | MODERATE | c.308C>T|p.Ser103Phe |
S295 |
| 157624 | BAA02g05300 | A02 | 2319007 | G | A | upstream_gene_variant | MODIFIER | c.-1536C>T| |
S297 |
| 157625 | BAA02g05310 | A02 | 2319347 | G | A | missense_variant | MODERATE | c.1700C>T|p.Pro567Leu |
S161 |