| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 153601 | BAA02g02030 | A02 | 906742 | G | A | upstream_gene_variant | MODIFIER | c.-4917C>T| |
S17 |
| 153602 | BAA02g02040 | A02 | 907933 | C | T | missense_variant | MODERATE | c.1775C>T|p.Ala592Val |
S56 |
| 153603 | BAA02g02040 | A02 | 908400 | G | A | missense_variant | MODERATE | c.1988G>A|p.Gly663Asp |
S67 |
| 153604 | BAA02g02040 | A02 | 909043 | C | T | splice_region_variant&intron_variant | LOW | c.2166-3C>T| |
S229 |
| 153605 | BAA02g02040 | A02 | 910901 | C | T | synonymous_variant | LOW | c.3150C>T|p.Phe1050Phe |
S94 |
| 153606 | BAA02g02040 | A02 | 910914 | G | A | downstream_gene_variant | MODIFIER | c.*1G>A| |
S293 |
| 153607 | BAA02g02050 | A02 | 912457 | G | A | missense_variant | MODERATE | c.467C>T|p.Thr156Ile |
S158 |
| 153608 | BAA02g02050 | A02 | 912962 | C | T | missense_variant | MODERATE | c.160G>A|p.Gly54Arg |
S123 |
| 153609 | BAA02g02050 | A02 | 914226 | G | A | upstream_gene_variant | MODIFIER | c.-1105C>T| |
S96 |
| 153610 | BAA02g02050 | A02 | 915813 | G | A | upstream_gene_variant | MODIFIER | c.-2692C>T| |
S236 |
| 153611 | BAA02g02060 | A02 | 917049 | C | T | missense_variant | MODERATE | c.1130G>A|p.Gly377Glu |
S167 |
| 153612 | BAA02g02060 | A02 | 917360 | C | T | missense_variant | MODERATE | c.913G>A|p.Glu305Lys |
S18 |
| 153613 | BAA02g02060 | A02 | 917964 | C | T | missense_variant | MODERATE | c.466G>A|p.Val156Ile |
S175 |
| 153614 | BAA02g02060 | A02 | 919369 | C | T | upstream_gene_variant | MODIFIER | c.-690G>A| |
S111 |
| 153615 | BAA02g02070 | A02 | 919674 | G | A | missense_variant | MODERATE | c.1498C>T|p.Leu500Phe |
S148 S210 S30 S31 |
| 153616 | BAA02g02070 | A02 | 920212 | C | T | missense_variant | MODERATE | c.1114G>A|p.Glu372Lys |
S160 |
| 153617 | BAA02g02070 | A02 | 920868 | G | A | splice_region_variant&intron_variant | LOW | c.795+8C>T| |
S273 |
| 153618 | BAA02g02070 | A02 | 921443 | C | T | splice_region_variant&synonymous_variant | LOW | c.537G>A|p.Arg179Arg |
S80 S85 |
| 153619 | BAA02g02070 | A02 | 921861 | C | T | missense_variant | MODERATE | c.295G>A|p.Glu99Lys |
S267 |
| 153620 | BAA02g02060 | A02 | 922811 | C | T | upstream_gene_variant | MODIFIER | c.-4132G>A| |
S277 |
| 153621 | BAA02g02070 | A02 | 924070 | C | T | upstream_gene_variant | MODIFIER | c.-1310G>A| |
S275 |
| 153622 | BAA02g02070 | A02 | 924125 | G | A | upstream_gene_variant | MODIFIER | c.-1365C>T| |
S256 |
| 153623 | BAA02g02070 | A02 | 924185 | C | T | upstream_gene_variant | MODIFIER | c.-1425G>A| |
S200 |
| 153624 | BAA02g02090 | A02 | 924734 | C | T | missense_variant | MODERATE | c.953G>A|p.Gly318Asp |
S8 |
| 153625 | BAA02g02090 | A02 | 926227 | G | A | missense_variant | MODERATE | c.140C>T|p.Ser47Phe |
S280 |