| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 18051 | BAA01g13520 | A01 | 6424164 | G | A | upstream_gene_variant | MODIFIER | c.-1980C>T| |
S274 |
| 18052 | BAA01g13520 | A01 | 6424329 | C | T | upstream_gene_variant | MODIFIER | c.-2145G>A| |
S192 |
| 18053 | BAA01g13520 | A01 | 6425638 | G | A | upstream_gene_variant | MODIFIER | c.-3454C>T| |
S122 |
| 18054 | BAA01g13520 | A01 | 6425649 | G | A | upstream_gene_variant | MODIFIER | c.-3465C>T| |
S13 |
| 18055 | BAA01g13530 | A01 | 6426019 | G | A | synonymous_variant | LOW | c.3325C>T|p.Leu1109Leu |
S199 |
| 18056 | BAA01g13530 | A01 | 6426824 | C | T | missense_variant | MODERATE | c.2731G>A|p.Val911Ile |
S150 |
| 18057 | BAA01g13530 | A01 | 6427380 | C | T | missense_variant | MODERATE | c.2437G>A|p.Gly813Ser |
S62 |
| 18058 | BAA01g13530 | A01 | 6427382 | C | T | missense_variant | MODERATE | c.2435G>A|p.Arg812His |
S136 |
| 18059 | BAA01g13530 | A01 | 6427576 | G | A | missense_variant | MODERATE | c.2326C>T|p.Leu776Phe |
S236 |
| 18060 | BAA01g13540 | A01 | 6427918 | G | A | upstream_gene_variant | MODIFIER | c.-4320G>A| |
S138 |
| 18061 | BAA01g13530 | A01 | 6428817 | C | T | missense_variant | MODERATE | c.1642G>A|p.Glu548Lys |
S265 |
| 18062 | BAA01g13530 | A01 | 6428825 | G | A | missense_variant | MODERATE | c.1634C>T|p.Pro545Leu |
S13 |
| 18063 | BAA01g13530 | A01 | 6429841 | C | T | missense_variant | MODERATE | c.1144G>A|p.Ala382Thr |
S128 |
| 18064 | BAA01g13530 | A01 | 6429848 | C | T | synonymous_variant | LOW | c.1137G>A|p.Leu379Leu |
S47 |
| 18065 | BAA01g13530 | A01 | 6430376 | C | T | missense_variant | MODERATE | c.913G>A|p.Glu305Lys |
S46 |
| 18066 | BAA01g13540 | A01 | 6431001 | C | T | upstream_gene_variant | MODIFIER | c.-1237C>T| |
S210 S225 |
| 18067 | BAA01g13540 | A01 | 6431382 | G | A | upstream_gene_variant | MODIFIER | c.-856G>A| |
S8 |
| 18068 | BAA01g13540 | A01 | 6433252 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.131-1G>A| |
S276 |
| 18069 | BAA01g13540 | A01 | 6433364 | C | T | splice_region_variant&intron_variant | LOW | c.234+8C>T| |
S38 |
| 18070 | BAA01g13530 | A01 | 6433385 | C | T | upstream_gene_variant | MODIFIER | c.-1450G>A| |
S69 |
| 18071 | BAA01g13540 | A01 | 6433468 | G | A | missense_variant | MODERATE | c.259G>A|p.Gly87Ser |
S298 |
| 18072 | BAA01g13540 | A01 | 6433661 | C | T | missense_variant | MODERATE | c.367C>T|p.Pro123Ser |
S44 |
| 18073 | BAA01g13550 | A01 | 6434518 | C | T | missense_variant | MODERATE | c.88C>T|p.Pro30Ser |
S239 S33 |
| 18074 | BAA01g13530 | A01 | 6435520 | G | A | upstream_gene_variant | MODIFIER | c.-3585C>T| |
S103 |
| 18075 | BAA01g13530 | A01 | 6436623 | G | A | upstream_gene_variant | MODIFIER | c.-4688C>T| |
S131 |