| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 172901 | BAA02g16540 | A02 | 8089718 | C | T | missense_variant | MODERATE | c.1124G>A|p.Arg375Lys |
S209 |
| 172902 | BAA02g16530 | A02 | 8091307 | C | T | upstream_gene_variant | MODIFIER | c.-4708G>A| |
S77 S82 |
| 172903 | BAA02g16540 | A02 | 8092127 | A | T | upstream_gene_variant | MODIFIER | c.-864T>A| |
S37 |
| 172904 | BAA02g16540 | A02 | 8092982 | G | A | upstream_gene_variant | MODIFIER | c.-1719C>T| |
S271 |
| 172905 | BAA02g16540 | A02 | 8093925 | C | T | upstream_gene_variant | MODIFIER | c.-2662G>A| |
S271 |
| 172906 | BAA02g16550 | A02 | 8094623 | G | A | synonymous_variant | LOW | c.1908C>T|p.Val636Val |
S223 |
| 172907 | BAA02g16550 | A02 | 8094668 | C | T | synonymous_variant | LOW | c.1863G>A|p.Lys621Lys |
S38 |
| 172908 | BAA02g16550 | A02 | 8094884 | C | T | stop_gained | HIGH | c.1647G>A|p.Trp549* |
S250 |
| 172909 | BAA02g16550 | A02 | 8095447 | C | T | missense_variant | MODERATE | c.1084G>A|p.Asp362Asn |
S72 S78 |
| 172910 | BAA02g16550 | A02 | 8095600 | T | G | missense_variant | MODERATE | c.931A>C|p.Lys311Gln |
S163 S7 S90 |
| 172911 | BAA02g16550 | A02 | 8095882 | G | A | missense_variant | MODERATE | c.649C>T|p.Pro217Ser |
S69 |
| 172912 | BAA02g16550 | A02 | 8096119 | C | T | missense_variant | MODERATE | c.488G>A|p.Ser163Asn |
S180 |
| 172913 | BAA02g16550 | A02 | 8096956 | G | A | stop_gained | HIGH | c.61C>T|p.Gln21* |
S166 |
| 172914 | BAA02g16550 | A02 | 8097285 | C | T | upstream_gene_variant | MODIFIER | c.-269G>A| |
S125 S162 S178 |
| 172915 | BAA02g16550 | A02 | 8100536 | G | A | upstream_gene_variant | MODIFIER | c.-3520C>T| |
S150 |
| 172916 | BAA02g16560 | A02 | 8102038 | C | T | upstream_gene_variant | MODIFIER | c.-960C>T| |
S163 |
| 172917 | BAA02g16560 | A02 | 8102713 | C | T | upstream_gene_variant | MODIFIER | c.-285C>T| |
S206 S26 |
| 172918 | BAA02g16560 | A02 | 8102720 | C | T | upstream_gene_variant | MODIFIER | c.-278C>T| |
S179 |
| 172919 | BAA02g16560 | A02 | 8103085 | C | T | synonymous_variant | LOW | c.88C>T|p.Leu30Leu |
S67 |
| 172920 | BAA02g16560 | A02 | 8103100 | G | A | missense_variant | MODERATE | c.103G>A|p.Glu35Lys |
S168 |
| 172921 | BAA02g16560 | A02 | 8103120 | G | A | synonymous_variant | LOW | c.123G>A|p.Val41Val |
S23 |
| 172922 | BAA02g16560 | A02 | 8103560 | G | A | missense_variant | MODERATE | c.563G>A|p.Arg188Lys |
S235 |
| 172923 | BAA02g16560 | A02 | 8104003 | G | A | missense_variant | MODERATE | c.917G>A|p.Ser306Asn |
S79 S91 |
| 172924 | BAA02g16560 | A02 | 8104281 | G | A | missense_variant | MODERATE | c.1133G>A|p.Arg378Lys |
S282 |
| 172925 | BAA02g16570 | A02 | 8104617 | C | T | upstream_gene_variant | MODIFIER | c.-664C>T| |
S211 S227 |