| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 170251 | BAA02g14980 | A02 | 7140107 | G | A | missense_variant | MODERATE | c.797C>T|p.Thr266Ile |
S61 |
| 170252 | BAA02g14980 | A02 | 7140431 | T | A | missense_variant | MODERATE | c.473A>T|p.Asp158Val |
S33 |
| 170253 | BAA02g14980 | A02 | 7140659 | G | A | missense_variant | MODERATE | c.245C>T|p.Thr82Ile |
S148 S210 |
| 170254 | BAA02g14970 | A02 | 7141255 | G | A | upstream_gene_variant | MODIFIER | c.-4215C>T| |
S282 |
| 170255 | BAA02g14970 | A02 | 7141284 | G | A | upstream_gene_variant | MODIFIER | c.-4244C>T| |
S246 |
| 170256 | BAA02g14980 | A02 | 7142123 | G | A | upstream_gene_variant | MODIFIER | c.-551C>T| |
S122 |
| 170257 | BAA02g14980 | A02 | 7142325 | C | T | upstream_gene_variant | MODIFIER | c.-753G>A| |
S216 |
| 170258 | BAA02g14980 | A02 | 7143740 | C | T | upstream_gene_variant | MODIFIER | c.-2168G>A| |
S202 |
| 170259 | BAA02g14990 | A02 | 7144194 | C | T | missense_variant | MODERATE | c.79C>T|p.Pro27Ser |
S302 |
| 170260 | BAA02g14980 | A02 | 7144364 | C | T | upstream_gene_variant | MODIFIER | c.-2792G>A| |
S216 |
| 170261 | BAA02g15000 | A02 | 7146754 | G | A | upstream_gene_variant | MODIFIER | c.-3274G>A| |
S303 |
| 170262 | BAA02g15000 | A02 | 7146947 | G | A | upstream_gene_variant | MODIFIER | c.-3081G>A| |
S125 |
| 170263 | BAA02g15000 | A02 | 7147473 | G | A | upstream_gene_variant | MODIFIER | c.-2555G>A| |
S157 |
| 170264 | BAA02g15000 | A02 | 7147864 | G | A | upstream_gene_variant | MODIFIER | c.-2164G>A| |
S157 |
| 170265 | BAA02g15000 | A02 | 7147980 | C | T | upstream_gene_variant | MODIFIER | c.-2048C>T| |
S15 S3 |
| 170266 | BAA02g14990 | A02 | 7148719 | C | T | synonymous_variant | LOW | c.1258C>T|p.Leu420Leu |
S115 |
| 170267 | BAA02g15000 | A02 | 7150202 | G | A | missense_variant | MODERATE | c.175G>A|p.Gly59Arg |
S184 |
| 170268 | BAA02g14990 | A02 | 7150562 | C | T | downstream_gene_variant | MODIFIER | c.*1107C>T| |
S138 |
| 170269 | BAA02g14990 | A02 | 7151795 | G | A | downstream_gene_variant | MODIFIER | c.*2340G>A| |
S28 |
| 170270 | BAA02g14990 | A02 | 7152441 | G | A | downstream_gene_variant | MODIFIER | c.*2986G>A| |
S187 |
| 170271 | BAA02g14990 | A02 | 7153655 | C | T | downstream_gene_variant | MODIFIER | c.*4200C>T| |
S305 |
| 170272 | BAA02g15000 | A02 | 7154619 | G | A | downstream_gene_variant | MODIFIER | c.*4343G>A| |
S87 |
| 170273 | BAA02g15000 | A02 | 7154774 | C | T | downstream_gene_variant | MODIFIER | c.*4498C>T| |
S302 |
| 170274 | BAA02g15000 | A02 | 7155247 | C | T | downstream_gene_variant | MODIFIER | c.*4971C>T| |
S71 |
| 170275 | BAA02g15010 | A02 | 7155950 | C | T | downstream_gene_variant | MODIFIER | c.*280G>A| |
S46 |