| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 84101 | BAA01g44560 | A01 | 29682563 | C | T | upstream_gene_variant | MODIFIER | c.-3605G>A| |
S97 |
| 84102 | BAA01g44560 | A01 | 29683088 | G | A | upstream_gene_variant | MODIFIER | c.-4130C>T| |
S138 S205 |
| 84103 | BAA01g44570 | A01 | 29684137 | C | T | upstream_gene_variant | MODIFIER | c.-869C>T| |
S73 S91 |
| 84104 | BAA01g44590 | A01 | 29691409 | G | A | upstream_gene_variant | MODIFIER | c.-33G>A| |
S278 |
| 84105 | BAA01g44590 | A01 | 29692697 | G | A | synonymous_variant | LOW | c.609G>A|p.Lys203Lys |
S232 |
| 84106 | BAA01g44590 | A01 | 29693036 | G | A | synonymous_variant | LOW | c.735G>A|p.Ala245Ala |
S302 S68 |
| 84107 | BAA01g44590 | A01 | 29693144 | C | T | synonymous_variant | LOW | c.843C>T|p.Ser281Ser |
S60 |
| 84108 | BAA01g44590 | A01 | 29693446 | C | T | missense_variant | MODERATE | c.1145C>T|p.Ser382Phe |
S77 S82 |
| 84109 | BAA01g44600 | A01 | 29693546 | G | A | upstream_gene_variant | MODIFIER | c.-4133G>A| |
S208 S219 |
| 84110 | BAA01g44600 | A01 | 29693551 | C | T | upstream_gene_variant | MODIFIER | c.-4128C>T| |
S37 |
| 84111 | BAA01g44590 | A01 | 29694487 | C | T | missense_variant | MODERATE | c.1867C>T|p.Pro623Ser |
S260 |
| 84112 | BAA01g44590 | A01 | 29695606 | C | T | missense_variant | MODERATE | c.2714C>T|p.Ala905Val |
S115 |
| 84113 | BAA01g44590 | A01 | 29695658 | G | A | synonymous_variant | LOW | c.2766G>A|p.Arg922Arg |
S217 S248 |
| 84114 | BAA01g44590 | A01 | 29695899 | G | A | missense_variant | MODERATE | c.3007G>A|p.Glu1003Lys |
S117 |
| 84115 | BAA01g44600 | A01 | 29697331 | G | A | upstream_gene_variant | MODIFIER | c.-348G>A| |
S53 |
| 84116 | BAA01g44600 | A01 | 29697612 | C | T | upstream_gene_variant | MODIFIER | c.-67C>T| |
S259 |
| 84117 | BAA01g44600 | A01 | 29697758 | C | T | missense_variant&splice_region_variant | MODERATE | c.80C>T|p.Ser27Phe |
S47 |
| 84118 | BAA01g44620 | A01 | 29698546 | G | A | upstream_gene_variant | MODIFIER | c.-4246G>A| |
S270 |
| 84119 | BAA01g44620 | A01 | 29698624 | C | T | upstream_gene_variant | MODIFIER | c.-4168C>T| |
S274 |
| 84120 | BAA01g44600 | A01 | 29699181 | C | T | missense_variant | MODERATE | c.976C>T|p.Leu326Phe |
S32 |
| 84121 | BAA01g44600 | A01 | 29699416 | G | A | missense_variant | MODERATE | c.1141G>A|p.Val381Ile |
S106 S185 |
| 84122 | BAA01g44620 | A01 | 29699679 | G | A | upstream_gene_variant | MODIFIER | c.-3113G>A| |
S181 |
| 84123 | BAA01g44600 | A01 | 29699795 | C | T | synonymous_variant | LOW | c.1363C>T|p.Leu455Leu |
S48 |
| 84124 | BAA01g44620 | A01 | 29700604 | G | A | upstream_gene_variant | MODIFIER | c.-2188G>A| |
S34 |
| 84125 | BAA01g44620 | A01 | 29700772 | C | T | upstream_gene_variant | MODIFIER | c.-2020C>T| |
S66 |