| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 195601 | BAA02g28620 | A02 | 16095810 | G | A | upstream_gene_variant | MODIFIER | c.-3029G>A| |
S129 |
| 195602 | BAA02g28620 | A02 | 16096034 | G | A | upstream_gene_variant | MODIFIER | c.-2805G>A| |
S103 |
| 195603 | BAA02g28620 | A02 | 16096073 | C | T | upstream_gene_variant | MODIFIER | c.-2766C>T| |
S16 |
| 195604 | BAA02g28620 | A02 | 16097222 | G | T | upstream_gene_variant | MODIFIER | c.-1617G>T| |
S278 |
| 195605 | BAA02g28620 | A02 | 16097444 | G | A | upstream_gene_variant | MODIFIER | c.-1395G>A| |
S256 |
| 195606 | BAA02g28620 | A02 | 16097715 | C | T | upstream_gene_variant | MODIFIER | c.-1124C>T| |
S245 |
| 195607 | BAA02g28610 | A02 | 16098255 | G | A | missense_variant | MODERATE | c.656G>A|p.Arg219Lys |
S229 |
| 195608 | BAA02g28610 | A02 | 16098576 | G | A | missense_variant | MODERATE | c.905G>A|p.Gly302Asp |
S113 |
| 195609 | BAA02g28620 | A02 | 16098713 | C | T | upstream_gene_variant | MODIFIER | c.-126C>T| |
S270 |
| 195610 | BAA02g28630 | A02 | 16098923 | G | A | upstream_gene_variant | MODIFIER | c.-4013G>A| |
S59 |
| 195611 | BAA02g28630 | A02 | 16100574 | C | T | upstream_gene_variant | MODIFIER | c.-2362C>T| |
S203 |
| 195612 | BAA02g28630 | A02 | 16101955 | G | A | upstream_gene_variant | MODIFIER | c.-981G>A| |
S298 |
| 195613 | BAA02g28630 | A02 | 16102167 | G | A | upstream_gene_variant | MODIFIER | c.-769G>A| |
S191 |
| 195614 | BAA02g28630 | A02 | 16102823 | G | A | upstream_gene_variant | MODIFIER | c.-113G>A| |
S217 |
| 195615 | BAA02g28630 | A02 | 16103012 | G | A | missense_variant | MODERATE | c.77G>A|p.Ser26Asn |
S134 |
| 195616 | BAA02g28630 | A02 | 16103979 | G | A | synonymous_variant | LOW | c.1044G>A|p.Gln348Gln |
S204 |
| 195617 | BAA02g28630 | A02 | 16104054 | G | A | synonymous_variant | LOW | c.1119G>A|p.Lys373Lys |
S207 |
| 195618 | BAA02g28630 | A02 | 16104351 | G | A | stop_gained | HIGH | c.1416G>A|p.Trp472* |
S259 |
| 195619 | BAA02g28630 | A02 | 16104740 | C | T | missense_variant | MODERATE | c.1805C>T|p.Pro602Leu |
S46 |
| 195620 | BAA02g28630 | A02 | 16105271 | C | T | missense_variant | MODERATE | c.2336C>T|p.Ser779Phe |
S105 S106 |
| 195621 | BAA02g28630 | A02 | 16105934 | G | A | missense_variant | MODERATE | c.2809G>A|p.Ala937Thr |
S143 |
| 195622 | BAA02g28630 | A02 | 16106183 | C | T | downstream_gene_variant | MODIFIER | c.*70C>T| |
S250 |
| 195623 | BAA02g28630 | A02 | 16106216 | C | T | downstream_gene_variant | MODIFIER | c.*103C>T| |
S194 |
| 195624 | BAA02g28630 | A02 | 16107495 | G | A | downstream_gene_variant | MODIFIER | c.*1382G>A| |
S36 |
| 195625 | BAA02g28630 | A02 | 16108344 | G | A | downstream_gene_variant | MODIFIER | c.*2231G>A| |
S110 |