| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 85701 | BAA01g45460 | A01 | 30311679 | C | T | missense_variant | MODERATE | c.775G>A|p.Gly259Arg |
S232 |
| 85702 | BAA01g45460 | A01 | 30311714 | C | T | missense_variant | MODERATE | c.740G>A|p.Arg247Lys |
S132 S215 S89 |
| 85703 | BAA01g45460 | A01 | 30311928 | C | T | missense_variant | MODERATE | c.526G>A|p.Glu176Lys |
S182 |
| 85704 | BAA01g45460 | A01 | 30312222 | C | T | missense_variant | MODERATE | c.232G>A|p.Glu78Lys |
S292 |
| 85705 | BAA01g45460 | A01 | 30312565 | G | A | upstream_gene_variant | MODIFIER | c.-112C>T| |
S187 |
| 85706 | BAA01g45460 | A01 | 30314446 | C | T | upstream_gene_variant | MODIFIER | c.-1993G>A| |
S16 |
| 85707 | BAA01g45460 | A01 | 30314826 | C | T | upstream_gene_variant | MODIFIER | c.-2373G>A| |
S201 |
| 85708 | BAA01g45460 | A01 | 30315115 | C | T | upstream_gene_variant | MODIFIER | c.-2662G>A| |
S183 S198 |
| 85709 | BAA01g45460 | A01 | 30315768 | G | A | upstream_gene_variant | MODIFIER | c.-3315C>T| |
S33 |
| 85710 | BAA01g45460 | A01 | 30315816 | C | T | upstream_gene_variant | MODIFIER | c.-3363G>A| |
S264 |
| 85711 | BAA01g45470 | A01 | 30316012 | C | T | stop_gained | HIGH | c.1325G>A|p.Trp442* |
S65 |
| 85712 | BAA01g45470 | A01 | 30316120 | C | T | missense_variant | MODERATE | c.1217G>A|p.Gly406Glu |
S27 |
| 85713 | BAA01g45470 | A01 | 30316130 | G | A | synonymous_variant | LOW | c.1207C>T|p.Leu403Leu |
S185 |
| 85714 | BAA01g45470 | A01 | 30316773 | G | A | synonymous_variant | LOW | c.648C>T|p.Pro216Pro |
S71 |
| 85715 | BAA01g45470 | A01 | 30319267 | C | T | upstream_gene_variant | MODIFIER | c.-1847G>A| |
S120 |
| 85716 | BAA01g45480 | A01 | 30319686 | C | T | missense_variant | MODERATE | c.74C>T|p.Ser25Phe |
S168 |
| 85717 | BAA01g45480 | A01 | 30320039 | G | A | missense_variant | MODERATE | c.427G>A|p.Glu143Lys |
S238 |
| 85718 | BAA01g45470 | A01 | 30320600 | G | A | upstream_gene_variant | MODIFIER | c.-3180C>T| |
S20 |
| 85719 | BAA01g45470 | A01 | 30320796 | G | A | upstream_gene_variant | MODIFIER | c.-3376C>T| |
S180 |
| 85720 | BAA01g45480 | A01 | 30323639 | G | A | downstream_gene_variant | MODIFIER | c.*3439G>A| |
S278 |
| 85721 | BAA01g45490 | A01 | 30323663 | G | A | missense_variant | MODERATE | c.647C>T|p.Ala216Val |
S152 |
| 85722 | BAA01g45490 | A01 | 30323783 | G | A | missense_variant | MODERATE | c.527C>T|p.Ser176Phe |
S13 |
| 85723 | BAA01g45490 | A01 | 30324394 | G | A | upstream_gene_variant | MODIFIER | c.-13C>T| |
S108 |
| 85724 | BAA01g45490 | A01 | 30325706 | C | T | upstream_gene_variant | MODIFIER | c.-1325G>A| |
S206 S26 |
| 85725 | BAA01g45490 | A01 | 30325723 | G | A | upstream_gene_variant | MODIFIER | c.-1342C>T| |
S47 |