| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 190501 | BAA02g25910 | A02 | 14359936 | C | T | upstream_gene_variant | MODIFIER | c.-3700C>T| |
S234 |
| 190502 | BAA02g25910 | A02 | 14360301 | C | T | upstream_gene_variant | MODIFIER | c.-3335C>T| |
S218 |
| 190503 | BAA02g25910 | A02 | 14360505 | C | T | upstream_gene_variant | MODIFIER | c.-3131C>T| |
S106 |
| 190504 | BAA02g25910 | A02 | 14362895 | G | A | upstream_gene_variant | MODIFIER | c.-741G>A| |
S197 |
| 190505 | BAA02g25910 | A02 | 14363099 | C | T | upstream_gene_variant | MODIFIER | c.-537C>T| |
S170 |
| 190506 | BAA02g25910 | A02 | 14363808 | G | A | missense_variant | MODERATE | c.173G>A|p.Arg58Lys |
S132 S137 S138 S215 S288 S89 |
| 190507 | BAA02g25910 | A02 | 14363847 | G | A | missense_variant | MODERATE | c.212G>A|p.Ser71Asn |
S7 |
| 190508 | BAA02g25910 | A02 | 14364356 | G | A | missense_variant | MODERATE | c.616G>A|p.Gly206Ser |
S306 |
| 190509 | BAA02g25910 | A02 | 14364360 | G | A | missense_variant | MODERATE | c.620G>A|p.Gly207Glu |
S5 |
| 190510 | BAA02g25910 | A02 | 14364546 | G | A | missense_variant | MODERATE | c.806G>A|p.Gly269Glu |
S20 |
| 190511 | BAA02g25920 | A02 | 14365086 | G | A | upstream_gene_variant | MODIFIER | c.-2661G>A| |
S298 |
| 190512 | BAA02g25920 | A02 | 14365430 | C | T | upstream_gene_variant | MODIFIER | c.-2317C>T| |
S252 |
| 190513 | BAA02g25920 | A02 | 14365431 | C | T | upstream_gene_variant | MODIFIER | c.-2316C>T| |
S106 |
| 190514 | BAA02g25920 | A02 | 14366415 | C | T | upstream_gene_variant | MODIFIER | c.-1332C>T| |
S25 S264 |
| 190515 | BAA02g25910 | A02 | 14369560 | C | T | downstream_gene_variant | MODIFIER | c.*4986C>T| |
S205 |
| 190516 | BAA02g25920 | A02 | 14369769 | C | T | missense_variant | MODERATE | c.811C>T|p.Pro271Ser |
S157 S163 |
| 190517 | BAA02g25920 | A02 | 14369852 | C | T | synonymous_variant | LOW | c.894C>T|p.Thr298Thr |
S205 |
| 190518 | BAA02g25920 | A02 | 14370575 | C | T | stop_gained | HIGH | c.1075C>T|p.Gln359* |
S192 |
| 190519 | BAA02g25920 | A02 | 14370773 | G | A | missense_variant | MODERATE | c.1195G>A|p.Gly399Arg |
S64 |
| 190520 | BAA02g25920 | A02 | 14372097 | G | A | missense_variant | MODERATE | c.1838G>A|p.Gly613Glu |
S251 |
| 190521 | BAA02g25920 | A02 | 14372331 | G | A | downstream_gene_variant | MODIFIER | c.*98G>A| |
S206 S26 |
| 190522 | BAA02g25920 | A02 | 14372658 | C | T | downstream_gene_variant | MODIFIER | c.*425C>T| |
S176 |
| 190523 | BAA02g25920 | A02 | 14372737 | C | T | downstream_gene_variant | MODIFIER | c.*504C>T| |
S5 |
| 190524 | BAA02g25920 | A02 | 14372916 | C | T | downstream_gene_variant | MODIFIER | c.*683C>T| |
S274 |
| 190525 | BAA02g25920 | A02 | 14373185 | G | A | downstream_gene_variant | MODIFIER | c.*952G>A| |
S175 |