| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 177201 | BAA02g18690 | A02 | 9605413 | G | A | upstream_gene_variant | MODIFIER | c.-3842C>T| |
S113 |
| 177202 | BAA02g18690 | A02 | 9605997 | C | T | upstream_gene_variant | MODIFIER | c.-4426G>A| |
S138 |
| 177203 | BAA02g18700 | A02 | 9607268 | C | T | upstream_gene_variant | MODIFIER | c.-3778G>A| |
S144 |
| 177204 | BAA02g18710 | A02 | 9614136 | T | A | intron_variant | MODIFIER | c.691+9A>T| |
S283 |
| 177205 | BAA02g18710 | A02 | 9614207 | G | A | missense_variant | MODERATE | c.629C>T|p.Pro210Leu |
S298 |
| 177206 | BAA02g18720 | A02 | 9614909 | G | A | upstream_gene_variant | MODIFIER | c.-4873G>A| |
S153 S213 |
| 177207 | BAA02g18720 | A02 | 9616086 | G | A | upstream_gene_variant | MODIFIER | c.-3696G>A| |
S79 S91 |
| 177208 | BAA02g18720 | A02 | 9616276 | C | T | upstream_gene_variant | MODIFIER | c.-3506C>T| |
S55 |
| 177209 | BAA02g18720 | A02 | 9616733 | G | A | upstream_gene_variant | MODIFIER | c.-3049G>A| |
S176 |
| 177210 | BAA02g18720 | A02 | 9616856 | G | A | upstream_gene_variant | MODIFIER | c.-2926G>A| |
S232 |
| 177211 | BAA02g18720 | A02 | 9617160 | C | T | upstream_gene_variant | MODIFIER | c.-2622C>T| |
S241 |
| 177212 | BAA02g18710 | A02 | 9618202 | C | T | upstream_gene_variant | MODIFIER | c.-596G>A| |
S255 S283 |
| 177213 | BAA02g18710 | A02 | 9618593 | G | A | upstream_gene_variant | MODIFIER | c.-987C>T| |
S240 |
| 177214 | BAA02g18710 | A02 | 9618655 | G | A | upstream_gene_variant | MODIFIER | c.-1049C>T| |
S169 |
| 177215 | BAA02g18710 | A02 | 9619355 | G | A | upstream_gene_variant | MODIFIER | c.-1749C>T| |
S169 |
| 177216 | BAA02g18710 | A02 | 9619428 | C | T | upstream_gene_variant | MODIFIER | c.-1822G>A| |
S266 |
| 177217 | BAA02g18710 | A02 | 9621271 | G | A | upstream_gene_variant | MODIFIER | c.-3665C>T| |
S162 |
| 177218 | BAA02g18710 | A02 | 9622262 | C | T | upstream_gene_variant | MODIFIER | c.-4656G>A| |
S58 |
| 177219 | BAA02g18730 | A02 | 9624318 | G | A | missense_variant | MODERATE | c.1216G>A|p.Ala406Thr |
S256 |
| 177220 | BAA02g18730 | A02 | 9624324 | G | A | missense_variant | MODERATE | c.1222G>A|p.Ala408Thr |
S53 |
| 177221 | BAA02g18730 | A02 | 9624334 | G | A | missense_variant | MODERATE | c.1232G>A|p.Arg411Lys |
S185 |
| 177222 | BAA02g18730 | A02 | 9624414 | G | A | missense_variant | MODERATE | c.1312G>A|p.Asp438Asn |
S62 |
| 177223 | BAA02g18720 | A02 | 9625162 | C | T | downstream_gene_variant | MODIFIER | c.*4130C>T| |
S104 S52 |
| 177224 | BAA02g18720 | A02 | 9625321 | G | A | downstream_gene_variant | MODIFIER | c.*4289G>A| |
S298 |
| 177225 | BAA02g18720 | A02 | 9625497 | G | A | downstream_gene_variant | MODIFIER | c.*4465G>A| |
S19 |