| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 11101 | BAA01g09020 | A01 | 3960325 | G | A | upstream_gene_variant | MODIFIER | c.-808C>T| |
S69 |
| 11102 | BAA01g09030 | A01 | 3960618 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.143-1G>A| |
S274 |
| 11103 | BAA01g09020 | A01 | 3960815 | C | T | upstream_gene_variant | MODIFIER | c.-1298G>A| |
S266 |
| 11104 | BAA01g09040 | A01 | 3961741 | G | A | missense_variant | MODERATE | c.4060C>T|p.Pro1354Ser |
S67 |
| 11105 | BAA01g09040 | A01 | 3961843 | C | T | missense_variant | MODERATE | c.3958G>A|p.Glu1320Lys |
S265 |
| 11106 | BAA01g09040 | A01 | 3963860 | G | A | synonymous_variant | LOW | c.2145C>T|p.Cys715Cys |
S34 |
| 11107 | BAA01g09040 | A01 | 3964546 | G | A | missense_variant | MODERATE | c.1459C>T|p.Pro487Ser |
S73 S91 |
| 11108 | BAA01g09040 | A01 | 3964611 | G | A | missense_variant | MODERATE | c.1394C>T|p.Ala465Val |
S10 |
| 11109 | BAA01g09040 | A01 | 3964777 | C | T | missense_variant | MODERATE | c.1228G>A|p.Asp410Asn |
S212 |
| 11110 | BAA01g09040 | A01 | 3964854 | G | A | missense_variant | MODERATE | c.1151C>T|p.Ser384Phe |
S239 |
| 11111 | BAA01g09050 | A01 | 3966387 | C | T | downstream_gene_variant | MODIFIER | c.*3096G>A| |
S43 |
| 11112 | BAA01g09040 | A01 | 3967285 | C | T | synonymous_variant | LOW | c.36G>A|p.Ser12Ser |
S48 |
| 11113 | BAA01g09040 | A01 | 3968424 | G | A | upstream_gene_variant | MODIFIER | c.-1104C>T| |
S202 |
| 11114 | BAA01g09040 | A01 | 3968785 | C | T | upstream_gene_variant | MODIFIER | c.-1465G>A| |
S296 |
| 11115 | BAA01g09040 | A01 | 3968910 | C | T | upstream_gene_variant | MODIFIER | c.-1590G>A| |
S282 |
| 11116 | BAA01g09050 | A01 | 3969831 | C | T | synonymous_variant | LOW | c.1899G>A|p.Lys633Lys |
S158 |
| 11117 | BAA01g09050 | A01 | 3969963 | G | A | synonymous_variant | LOW | c.1767C>T|p.Asp589Asp |
S180 |
| 11118 | BAA01g09050 | A01 | 3972165 | C | T | splice_region_variant&intron_variant | LOW | c.463+6G>A| |
S244 |
| 11119 | BAA01g09050 | A01 | 3972210 | G | A | missense_variant | MODERATE | c.424C>T|p.Leu142Phe |
S163 |
| 11120 | BAA01g09050 | A01 | 3974393 | C | T | upstream_gene_variant | MODIFIER | c.-856G>A| |
S267 |
| 11121 | BAA01g09050 | A01 | 3975469 | G | A | upstream_gene_variant | MODIFIER | c.-1932C>T| |
S149 |
| 11122 | BAA01g09060 | A01 | 3976383 | C | T | missense_variant | MODERATE | c.676G>A|p.Asp226Asn |
S38 |
| 11123 | BAA01g09060 | A01 | 3977014 | G | A | missense_variant | MODERATE | c.149C>T|p.Ser50Phe |
S162 |
| 11124 | BAA01g09050 | A01 | 3977376 | G | A | upstream_gene_variant | MODIFIER | c.-3839C>T| |
S117 |
| 11125 | BAA01g09070 | A01 | 3977643 | G | A | synonymous_variant | LOW | c.972C>T|p.Val324Val |
S275 |