| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 74351 | BAA01g39080 | A01 | 26011833 | C | T | upstream_gene_variant | MODIFIER | c.-4745G>A| |
S221 |
| 74352 | BAA01g39090 | A01 | 26012258 | C | T | downstream_gene_variant | MODIFIER | c.*2237G>A| |
S305 |
| 74353 | BAA01g39090 | A01 | 26012559 | C | T | downstream_gene_variant | MODIFIER | c.*1936G>A| |
S148 S30 S31 |
| 74354 | BAA01g39090 | A01 | 26012728 | C | T | downstream_gene_variant | MODIFIER | c.*1767G>A| |
S293 |
| 74355 | BAA01g39090 | A01 | 26013660 | C | T | downstream_gene_variant | MODIFIER | c.*835G>A| |
S134 |
| 74356 | BAA01g39100 | A01 | 26014184 | C | T | upstream_gene_variant | MODIFIER | c.-4742C>T| |
S234 |
| 74357 | BAA01g39090 | A01 | 26016687 | G | A | upstream_gene_variant | MODIFIER | c.-707C>T| |
S308 |
| 74358 | BAA01g39090 | A01 | 26017121 | G | A | upstream_gene_variant | MODIFIER | c.-1141C>T| |
S55 |
| 74359 | BAA01g39090 | A01 | 26017197 | G | A | upstream_gene_variant | MODIFIER | c.-1217C>T| |
S208 |
| 74360 | BAA01g39090 | A01 | 26017815 | C | T | upstream_gene_variant | MODIFIER | c.-1835G>A| |
S159 S243 |
| 74361 | BAA01g39090 | A01 | 26018493 | G | A | upstream_gene_variant | MODIFIER | c.-2513C>T| |
S8 |
| 74362 | BAA01g39100 | A01 | 26019882 | C | T | synonymous_variant | LOW | c.957C>T|p.Cys319Cys |
S200 |
| 74363 | BAA01g39100 | A01 | 26019998 | C | T | missense_variant | MODERATE | c.1073C>T|p.Ser358Phe |
S50 |
| 74364 | BAA01g39100 | A01 | 26019999 | C | T | synonymous_variant | LOW | c.1074C>T|p.Ser358Ser |
S9 |
| 74365 | BAA01g39100 | A01 | 26020035 | G | A | stop_gained | HIGH | c.1110G>A|p.Trp370* |
S246 |
| 74366 | BAA01g39100 | A01 | 26020328 | C | T | missense_variant | MODERATE | c.1403C>T|p.Ser468Leu |
S270 |
| 74367 | BAA01g39100 | A01 | 26020893 | G | A | stop_gained | HIGH | c.1968G>A|p.Trp656* |
S117 |
| 74368 | BAA01g39100 | A01 | 26021041 | C | T | missense_variant | MODERATE | c.2021C>T|p.Ala674Val |
S56 |
| 74369 | BAA01g39100 | A01 | 26021601 | G | A | downstream_gene_variant | MODIFIER | c.*553G>A| |
S1 S90 |
| 74370 | BAA01g39110 | A01 | 26022476 | C | T | missense_variant | MODERATE | c.1183G>A|p.Gly395Arg |
S39 |
| 74371 | BAA01g39110 | A01 | 26023218 | C | T | synonymous_variant | LOW | c.441G>A|p.Gly147Gly |
S171 |
| 74372 | BAA01g39110 | A01 | 26023306 | C | T | missense_variant | MODERATE | c.353G>A|p.Cys118Tyr |
S270 |
| 74373 | BAA01g39110 | A01 | 26024078 | C | T | upstream_gene_variant | MODIFIER | c.-420G>A| |
S171 |
| 74374 | BAA01g39110 | A01 | 26024092 | G | A | upstream_gene_variant | MODIFIER | c.-434C>T| |
S36 |
| 74375 | BAA01g39110 | A01 | 26024221 | G | A | upstream_gene_variant | MODIFIER | c.-563C>T| |
S123 |