| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 159501 | BAA02g06860 | A02 | 2943025 | G | A | upstream_gene_variant | MODIFIER | c.-1304G>A| |
S287 |
| 159502 | BAA02g06860 | A02 | 2943315 | C | T | upstream_gene_variant | MODIFIER | c.-1014C>T| |
S34 |
| 159503 | BAA02g06860 | A02 | 2944086 | G | A | upstream_gene_variant | MODIFIER | c.-243G>A| |
S48 |
| 159504 | BAA02g06860 | A02 | 2945057 | C | T | synonymous_variant | LOW | c.417C>T|p.Val139Val |
S224 |
| 159505 | BAA02g06860 | A02 | 2946841 | G | A | synonymous_variant | LOW | c.1092G>A|p.Val364Val |
S288 |
| 159506 | BAA02g06860 | A02 | 2946877 | G | A | splice_region_variant&intron_variant | LOW | c.1125+3G>A| |
S57 |
| 159507 | BAA02g06860 | A02 | 2947861 | G | A | splice_region_variant&synonymous_variant | LOW | c.1347G>A|p.Val449Val |
S156 |
| 159508 | BAA02g06860 | A02 | 2948485 | G | A | downstream_gene_variant | MODIFIER | c.*543G>A| |
S132 |
| 159509 | BAA02g06870 | A02 | 2948948 | G | A | synonymous_variant | LOW | c.1086C>T|p.Leu362Leu |
S232 |
| 159510 | BAA02g06870 | A02 | 2949075 | C | T | missense_variant | MODERATE | c.959G>A|p.Gly320Glu |
S55 |
| 159511 | BAA02g06870 | A02 | 2950417 | G | A | synonymous_variant | LOW | c.309C>T|p.Leu103Leu |
S273 |
| 159512 | BAA02g06870 | A02 | 2950517 | C | T | missense_variant | MODERATE | c.209G>A|p.Gly70Glu |
S241 |
| 159513 | BAA02g06870 | A02 | 2950856 | G | A | upstream_gene_variant | MODIFIER | c.-44C>T| |
S34 |
| 159514 | BAA02g06880 | A02 | 2951678 | C | T | synonymous_variant | LOW | c.1353G>A|p.Glu451Glu |
S66 |
| 159515 | BAA02g06880 | A02 | 2952493 | G | A | missense_variant | MODERATE | c.538C>T|p.Pro180Ser |
S132 |
| 159516 | BAA02g06880 | A02 | 2952505 | C | T | missense_variant | MODERATE | c.526G>A|p.Val176Ile |
S34 |
| 159517 | BAA02g06880 | A02 | 2952730 | C | T | missense_variant | MODERATE | c.301G>A|p.Gly101Arg |
S88 |
| 159518 | BAA02g06890 | A02 | 2955258 | G | A | stop_gained | HIGH | c.694C>T|p.Gln232* |
S144 |
| 159519 | BAA02g06870 | A02 | 2955427 | G | A | upstream_gene_variant | MODIFIER | c.-4615C>T| |
S265 |
| 159520 | BAA02g06890 | A02 | 2955685 | G | A | missense_variant | MODERATE | c.595C>T|p.Leu199Phe |
S165 |
| 159521 | BAA02g06890 | A02 | 2955877 | C | T | missense_variant | MODERATE | c.403G>A|p.Asp135Asn |
S19 |
| 159522 | BAA02g06890 | A02 | 2956632 | G | A | synonymous_variant | LOW | c.24C>T|p.Leu8Leu |
S84 S93 |
| 159523 | BAA02g06890 | A02 | 2959390 | C | T | upstream_gene_variant | MODIFIER | c.-2735G>A| |
S124 |
| 159524 | BAA02g06910 | A02 | 2961307 | C | T | synonymous_variant | LOW | c.279G>A|p.Glu93Glu |
S78 S79 |
| 159525 | BAA02g06910 | A02 | 2961321 | G | A | missense_variant | MODERATE | c.265C>T|p.Pro89Ser |
S11 |