| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 39301 | BAA01g25210-BAA01g25220 | A01 | 13567365 | C | T | intergenic_region | MODIFIER | n.13567365C>T| |
S125 |
| 39302 | BAA01g25220 | A01 | 13568973 | G | A | downstream_gene_variant | MODIFIER | c.*3442C>T| |
S58 |
| 39303 | BAA01g25220 | A01 | 13569251 | G | A | downstream_gene_variant | MODIFIER | c.*3164C>T| |
S274 |
| 39304 | BAA01g25220 | A01 | 13570212 | G | A | downstream_gene_variant | MODIFIER | c.*2203C>T| |
S244 |
| 39305 | BAA01g25220 | A01 | 13571949 | C | T | downstream_gene_variant | MODIFIER | c.*466G>A| |
S16 |
| 39306 | BAA01g25220 | A01 | 13572323 | G | A | downstream_gene_variant | MODIFIER | c.*92C>T| |
S58 |
| 39307 | BAA01g25220 | A01 | 13572409 | C | T | downstream_gene_variant | MODIFIER | c.*6G>A| |
S183 |
| 39308 | BAA01g25220 | A01 | 13572529 | G | A | missense_variant | MODERATE | c.856C>T|p.Leu286Phe |
S17 |
| 39309 | BAA01g25220 | A01 | 13572956 | C | T | synonymous_variant | LOW | c.429G>A|p.Lys143Lys |
S279 |
| 39310 | BAA01g25220 | A01 | 13573015 | C | T | missense_variant | MODERATE | c.370G>A|p.Val124Ile |
S162 |
| 39311 | BAA01g25220 | A01 | 13574294 | C | T | upstream_gene_variant | MODIFIER | c.-910G>A| |
S11 |
| 39312 | BAA01g25220 | A01 | 13574412 | G | A | upstream_gene_variant | MODIFIER | c.-1028C>T| |
S235 |
| 39313 | BAA01g25220 | A01 | 13575519 | C | T | upstream_gene_variant | MODIFIER | c.-2135G>A| |
S17 |
| 39314 | BAA01g25220 | A01 | 13576840 | G | A | upstream_gene_variant | MODIFIER | c.-3456C>T| |
S298 |
| 39315 | BAA01g25220 | A01 | 13577456 | G | A | upstream_gene_variant | MODIFIER | c.-4072C>T| |
S86 |
| 39316 | BAA01g25220 | A01 | 13577635 | G | A | upstream_gene_variant | MODIFIER | c.-4251C>T| |
S195 |
| 39317 | BAA01g25220 | A01 | 13577672 | G | A | upstream_gene_variant | MODIFIER | c.-4288C>T| |
S126 |
| 39318 | BAA01g25230 | A01 | 13578028 | C | T | synonymous_variant | LOW | c.2022G>A|p.Gln674Gln |
S203 |
| 39319 | BAA01g25230 | A01 | 13578210 | G | A | missense_variant | MODERATE | c.1840C>T|p.Leu614Phe |
S34 |
| 39320 | BAA01g25230 | A01 | 13580823 | G | A | intron_variant | MODIFIER | c.1228-71C>T| |
S294 |
| 39321 | BAA01g25230 | A01 | 13580832 | G | A | intron_variant | MODIFIER | c.1228-80C>T| |
S71 |
| 39322 | BAA01g25230 | A01 | 13581186 | G | A | splice_region_variant&intron_variant | LOW | c.979-8C>T| |
S7 |
| 39323 | BAA01g25230 | A01 | 13581382 | G | A | missense_variant | MODERATE | c.899C>T|p.Ala300Val |
S208 |
| 39324 | BAA01g25230 | A01 | 13583348 | C | T | upstream_gene_variant | MODIFIER | c.-208G>A| |
S128 |
| 39325 | BAA01g25230 | A01 | 13583486 | A | G | upstream_gene_variant | MODIFIER | c.-346T>C| |
S146 |