| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 177801 | BAA02g19000 | A02 | 9822535 | G | A | upstream_gene_variant | MODIFIER | c.-495C>T| |
S64 |
| 177802 | BAA02g19000 | A02 | 9822622 | G | A | upstream_gene_variant | MODIFIER | c.-582C>T| |
S41 |
| 177803 | BAA02g19000 | A02 | 9824081 | G | A | upstream_gene_variant | MODIFIER | c.-2041C>T| |
S169 |
| 177804 | BAA02g19000 | A02 | 9824125 | C | T | upstream_gene_variant | MODIFIER | c.-2085G>A| |
S292 |
| 177805 | BAA02g19000 | A02 | 9824144 | C | T | upstream_gene_variant | MODIFIER | c.-2104G>A| |
S183 S198 |
| 177806 | BAA02g19000 | A02 | 9826258 | G | A | upstream_gene_variant | MODIFIER | c.-4218C>T| |
S12 |
| 177807 | BAA02g19010 | A02 | 9827830 | C | T | intron_variant | MODIFIER | c.352+48C>T| |
S308 |
| 177808 | BAA02g19010 | A02 | 9828620 | C | T | missense_variant | MODERATE | c.725C>T|p.Thr242Ile |
S76 |
| 177809 | BAA02g19010 | A02 | 9828782 | C | T | missense_variant | MODERATE | c.811C>T|p.Leu271Phe |
S40 S49 |
| 177810 | BAA02g19020 | A02 | 9831223 | G | A | upstream_gene_variant | MODIFIER | c.-4418G>A| |
S5 |
| 177811 | BAA02g19020 | A02 | 9831751 | C | T | upstream_gene_variant | MODIFIER | c.-3890C>T| |
S75 S81 |
| 177812 | BAA02g19020 | A02 | 9832430 | C | A | upstream_gene_variant | MODIFIER | c.-3211C>A| |
S136 S202 S53 |
| 177813 | BAA02g19020 | A02 | 9834319 | G | A | upstream_gene_variant | MODIFIER | c.-1322G>A| |
S162 |
| 177814 | BAA02g19020 | A02 | 9834491 | C | T | upstream_gene_variant | MODIFIER | c.-1150C>T| |
S221 |
| 177815 | BAA02g19020 | A02 | 9837180 | C | T | intron_variant | MODIFIER | c.379+1161C>T| |
S277 |
| 177816 | BAA02g19020 | A02 | 9838610 | G | A | intron_variant | MODIFIER | c.380-95G>A| |
S70 |
| 177817 | BAA02g19020 | A02 | 9838936 | C | T | missense_variant | MODERATE | c.611C>T|p.Ser204Phe |
S202 |
| 177818 | BAA02g19020 | A02 | 9839137 | G | A | synonymous_variant | LOW | c.714G>A|p.Thr238Thr |
S158 |
| 177819 | BAA02g19020 | A02 | 9839491 | G | A | missense_variant | MODERATE | c.980G>A|p.Arg327Lys |
S129 |
| 177820 | BAA02g19030 | A02 | 9840061 | C | T | downstream_gene_variant | MODIFIER | c.*4093G>A| |
S16 |
| 177821 | BAA02g19030 | A02 | 9840812 | C | T | downstream_gene_variant | MODIFIER | c.*3342G>A| |
S158 |
| 177822 | BAA02g19020 | A02 | 9841499 | C | T | synonymous_variant | LOW | c.2253C>T|p.Ile751Ile |
S103 |
| 177823 | BAA02g19020 | A02 | 9843182 | C | T | downstream_gene_variant | MODIFIER | c.*1194C>T| |
S104 S52 |
| 177824 | BAA02g19020 | A02 | 9843348 | C | T | downstream_gene_variant | MODIFIER | c.*1360C>T| |
S42 |
| 177825 | BAA02g19020 | A02 | 9843812 | G | A | downstream_gene_variant | MODIFIER | c.*1824G>A| |
S217 S248 |