| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 215651 | BAA02g32200 | A02 | 27122204 | C | T | intron_variant | MODIFIER | c.377+610C>T| |
S114 |
| 215652 | BAA02g32200 | A02 | 27122259 | C | T | intron_variant | MODIFIER | c.377+665C>T| |
S79 S91 |
| 215653 | BAA02g32200 | A02 | 27122859 | G | A | intron_variant | MODIFIER | c.377+1265G>A| |
S247 |
| 215654 | BAA02g32200 | A02 | 27123547 | C | T | intron_variant | MODIFIER | c.378-733C>T| |
S295 |
| 215655 | BAA02g32200 | A02 | 27123732 | G | A | intron_variant | MODIFIER | c.378-548G>A| |
S69 |
| 215656 | BAA02g32200 | A02 | 27124629 | C | A | missense_variant | MODERATE | c.630C>A|p.His210Gln |
S292 |
| 215657 | BAA02g32200 | A02 | 27126007 | C | T | missense_variant | MODERATE | c.1348C>T|p.Leu450Phe |
S64 |
| 215658 | BAA02g32200 | A02 | 27126070 | G | A | missense_variant | MODERATE | c.1411G>A|p.Gly471Arg |
S103 |
| 215659 | BAA02g32200 | A02 | 27126228 | C | T | synonymous_variant | LOW | c.1569C>T|p.Val523Val |
S116 S34 |
| 215660 | BAA02g32210 | A02 | 27126441 | C | T | upstream_gene_variant | MODIFIER | c.-4897C>T| |
S94 |
| 215661 | BAA02g32210 | A02 | 27129055 | C | T | upstream_gene_variant | MODIFIER | c.-2283C>T| |
S59 |
| 215662 | BAA02g32210 | A02 | 27129268 | C | T | upstream_gene_variant | MODIFIER | c.-2070C>T| |
S271 |
| 215663 | BAA02g32210 | A02 | 27130542 | C | T | upstream_gene_variant | MODIFIER | c.-796C>T| |
S105 S106 |
| 215664 | BAA02g32210 | A02 | 27131625 | C | T | splice_region_variant&intron_variant | LOW | c.160-3C>T| |
S42 |
| 215665 | BAA02g32210 | A02 | 27131777 | G | A | synonymous_variant | LOW | c.309G>A|p.Arg103Arg |
S47 |
| 215666 | BAA02g32210 | A02 | 27132027 | G | A | missense_variant | MODERATE | c.559G>A|p.Gly187Ser |
S288 |
| 215667 | BAA02g32210 | A02 | 27132165 | G | A | missense_variant | MODERATE | c.697G>A|p.Gly233Ser |
S281 |
| 215668 | BAA02g32210 | A02 | 27132678 | G | A | missense_variant | MODERATE | c.1210G>A|p.Val404Ile |
S125 |
| 215669 | BAA02g32210 | A02 | 27133003 | C | T | intron_variant | MODIFIER | c.1370+83C>T| |
S212 |
| 215670 | BAA02g32220 | A02 | 27133157 | C | T | downstream_gene_variant | MODIFIER | c.*4966G>A| |
S124 |
| 215671 | BAA02g32210 | A02 | 27133655 | G | A | missense_variant | MODERATE | c.1763G>A|p.Arg588Lys |
S146 |
| 215672 | BAA02g32210 | A02 | 27133740 | G | A | synonymous_variant | LOW | c.1848G>A|p.Glu616Glu |
S23 |
| 215673 | BAA02g32210 | A02 | 27134325 | C | T | downstream_gene_variant | MODIFIER | c.*130C>T| |
S180 |
| 215674 | BAA02g32210 | A02 | 27134958 | G | A | downstream_gene_variant | MODIFIER | c.*763G>A| |
S236 |
| 215675 | BAA02g32210 | A02 | 27135237 | C | T | downstream_gene_variant | MODIFIER | c.*1042C>T| |
S177 |