| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 170601 | BAA02g15140 | A02 | 7267418 | G | A | intron_variant | MODIFIER | c.853-21C>T| |
S303 |
| 170602 | BAA02g15140 | A02 | 7267885 | C | T | missense_variant | MODERATE | c.670G>A|p.Gly224Arg |
S221 |
| 170603 | BAA02g15140 | A02 | 7268351 | C | T | missense_variant | MODERATE | c.401G>A|p.Gly134Asp |
S39 |
| 170604 | BAA02g15140 | A02 | 7268418 | G | A | missense_variant | MODERATE | c.334C>T|p.Leu112Phe |
S289 S290 |
| 170605 | BAA02g15140 | A02 | 7268546 | G | A | synonymous_variant | LOW | c.291C>T|p.Leu97Leu |
S289 S290 |
| 170606 | BAA02g15140 | A02 | 7268783 | G | A | synonymous_variant | LOW | c.144C>T|p.Asn48Asn |
S184 |
| 170607 | BAA02g15140 | A02 | 7268828 | G | A | synonymous_variant | LOW | c.99C>T|p.Tyr33Tyr |
S281 |
| 170608 | BAA02g15140 | A02 | 7269729 | G | A | upstream_gene_variant | MODIFIER | c.-803C>T| |
S144 |
| 170609 | BAA02g15140 | A02 | 7269767 | C | G | upstream_gene_variant | MODIFIER | c.-841G>C| |
S46 |
| 170610 | BAA02g15140 | A02 | 7269837 | G | A | upstream_gene_variant | MODIFIER | c.-911C>T| |
S159 S243 |
| 170611 | BAA02g15140 | A02 | 7270410 | C | T | upstream_gene_variant | MODIFIER | c.-1484G>A| |
S88 |
| 170612 | BAA02g15140 | A02 | 7270558 | G | A | upstream_gene_variant | MODIFIER | c.-1632C>T| |
S298 |
| 170613 | BAA02g15140 | A02 | 7270789 | G | A | upstream_gene_variant | MODIFIER | c.-1863C>T| |
S134 |
| 170614 | BAA02g15140 | A02 | 7270925 | G | A | upstream_gene_variant | MODIFIER | c.-1999C>T| |
S47 |
| 170615 | BAA02g15140 | A02 | 7271617 | C | T | upstream_gene_variant | MODIFIER | c.-2691G>A| |
S301 S304 |
| 170616 | BAA02g15140 | A02 | 7272111 | G | A | upstream_gene_variant | MODIFIER | c.-3185C>T| |
S296 |
| 170617 | BAA02g15140 | A02 | 7272581 | C | T | upstream_gene_variant | MODIFIER | c.-3655G>A| |
S130 |
| 170618 | BAA02g15140 | A02 | 7272622 | G | A | upstream_gene_variant | MODIFIER | c.-3696C>T| |
S293 |
| 170619 | BAA02g15160 | A02 | 7274710 | G | A | upstream_gene_variant | MODIFIER | c.-2268G>A| |
S184 |
| 170620 | BAA02g15150 | A02 | 7275008 | G | A | missense_variant | MODERATE | c.142C>T|p.Arg48Trp |
S161 |
| 170621 | BAA02g15150 | A02 | 7275199 | C | T | upstream_gene_variant | MODIFIER | c.-50G>A| |
S12 |
| 170622 | BAA02g15150 | A02 | 7275841 | G | A | upstream_gene_variant | MODIFIER | c.-692C>T| |
S28 |
| 170623 | BAA02g15160 | A02 | 7277024 | G | A | missense_variant | MODERATE | c.47G>A|p.Arg16Lys |
S10 |
| 170624 | BAA02g15150 | A02 | 7277264 | G | A | upstream_gene_variant | MODIFIER | c.-2115C>T| |
S183 S198 |
| 170625 | BAA02g15160 | A02 | 7277427 | G | A | missense_variant | MODERATE | c.376G>A|p.Gly126Arg |
S133 |