| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 151951 | BAA02g00530 | A02 | 297061 | C | T | downstream_gene_variant | MODIFIER | c.*3150C>T| |
S301 S304 |
| 151952 | BAA02g00540 | A02 | 304812 | C | T | upstream_gene_variant | MODIFIER | c.-1937G>A| |
S135 |
| 151953 | BAA02g00540 | A02 | 305136 | G | A | upstream_gene_variant | MODIFIER | c.-2261C>T| |
S215 |
| 151954 | BAA02g00540 | A02 | 306812 | C | T | upstream_gene_variant | MODIFIER | c.-3937G>A| |
S278 |
| 151955 | BAA02g00550 | A02 | 308521 | G | A | upstream_gene_variant | MODIFIER | c.-1723C>T| |
S84 S93 |
| 151956 | BAA02g00550 | A02 | 308869 | G | A | upstream_gene_variant | MODIFIER | c.-2071C>T| |
S295 |
| 151957 | BAA02g00550 | A02 | 308956 | C | T | upstream_gene_variant | MODIFIER | c.-2158G>A| |
S186 |
| 151958 | BAA02g00560 | A02 | 309284 | C | T | missense_variant | MODERATE | c.205C>T|p.Pro69Ser |
S218 |
| 151959 | BAA02g00550 | A02 | 310789 | C | T | upstream_gene_variant | MODIFIER | c.-3991G>A| |
S182 |
| 151960 | BAA02g00560 | A02 | 311200 | G | A | splice_region_variant&intron_variant | LOW | c.1400-5G>A| |
S169 |
| 151961 | BAA02g00580 | A02 | 312246 | C | T | upstream_gene_variant | MODIFIER | c.-4573C>T| |
S216 |
| 151962 | BAA02g00580 | A02 | 312291 | C | T | upstream_gene_variant | MODIFIER | c.-4528C>T| |
S207 |
| 151963 | BAA02g00580 | A02 | 312630 | G | A | upstream_gene_variant | MODIFIER | c.-4189G>A| |
S128 |
| 151964 | BAA02g00580 | A02 | 312866 | G | A | upstream_gene_variant | MODIFIER | c.-3953G>A| |
S64 |
| 151965 | BAA02g00580 | A02 | 316917 | G | A | synonymous_variant | LOW | c.99G>A|p.Gln33Gln |
S295 |
| 151966 | BAA02g00570 | A02 | 317132 | G | A | upstream_gene_variant | MODIFIER | c.-2826C>T| |
S244 |
| 151967 | BAA02g00580 | A02 | 317507 | C | T | synonymous_variant | LOW | c.375C>T|p.Leu125Leu |
S85 |
| 151968 | BAA02g00580 | A02 | 317578 | C | T | missense_variant | MODERATE | c.446C>T|p.Pro149Leu |
S251 |
| 151969 | BAA02g00570 | A02 | 317785 | G | A | upstream_gene_variant | MODIFIER | c.-3479C>T| |
S140 |
| 151970 | BAA02g00580 | A02 | 318118 | G | A | missense_variant | MODERATE | c.614G>A|p.Arg205Lys |
S4 |
| 151971 | BAA02g00580 | A02 | 318656 | C | T | missense_variant | MODERATE | c.829C>T|p.Pro277Ser |
S201 |
| 151972 | BAA02g00580 | A02 | 318671 | G | A | missense_variant | MODERATE | c.844G>A|p.Gly282Arg |
S87 |
| 151973 | BAA02g00570 | A02 | 319012 | G | A | upstream_gene_variant | MODIFIER | c.-4706C>T| |
S127 |
| 151974 | BAA02g00580 | A02 | 319739 | G | A | downstream_gene_variant | MODIFIER | c.*913G>A| |
S188 |
| 151975 | BAA02g00580 | A02 | 319764 | C | T | downstream_gene_variant | MODIFIER | c.*938C>T| |
S228 |