| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 183501 | BAA02g22080 | A02 | 11892427 | G | A | splice_region_variant&intron_variant | LOW | c.1719+5G>A| |
S298 |
| 183502 | BAA02g22080 | A02 | 11892540 | G | A | synonymous_variant | LOW | c.1740G>A|p.Ala580Ala |
S212 |
| 183503 | BAA02g22080 | A02 | 11892556 | C | T | synonymous_variant | LOW | c.1756C>T|p.Leu586Leu |
S242 |
| 183504 | BAA02g22080 | A02 | 11894353 | G | A | downstream_gene_variant | MODIFIER | c.*768G>A| |
S70 |
| 183505 | BAA02g22080 | A02 | 11895150 | C | T | downstream_gene_variant | MODIFIER | c.*1565C>T| |
S99 |
| 183506 | BAA02g22080 | A02 | 11895245 | G | A | downstream_gene_variant | MODIFIER | c.*1660G>A| |
S59 |
| 183507 | BAA02g22090 | A02 | 11895367 | G | A | synonymous_variant | LOW | c.1704C>T|p.Val568Val |
S156 |
| 183508 | BAA02g22090 | A02 | 11895816 | C | T | missense_variant | MODERATE | c.1255G>A|p.Glu419Lys |
S276 |
| 183509 | BAA02g22080 | A02 | 11896284 | C | T | downstream_gene_variant | MODIFIER | c.*2699C>T| |
S186 |
| 183510 | BAA02g22080 | A02 | 11896676 | C | T | downstream_gene_variant | MODIFIER | c.*3091C>T| |
S157 S163 |
| 183511 | BAA02g22080 | A02 | 11896712 | C | T | downstream_gene_variant | MODIFIER | c.*3127C>T| |
S20 |
| 183512 | BAA02g22080 | A02 | 11897052 | G | A | downstream_gene_variant | MODIFIER | c.*3467G>A| |
S109 |
| 183513 | BAA02g22080 | A02 | 11897151 | C | T | downstream_gene_variant | MODIFIER | c.*3566C>T| |
S270 |
| 183514 | BAA02g22080 | A02 | 11897173 | C | T | downstream_gene_variant | MODIFIER | c.*3588C>T| |
S123 |
| 183515 | BAA02g22080 | A02 | 11898023 | G | A | downstream_gene_variant | MODIFIER | c.*4438G>A| |
S111 |
| 183516 | BAA02g22080 | A02 | 11898166 | C | T | downstream_gene_variant | MODIFIER | c.*4581C>T| |
S219 |
| 183517 | BAA02g22080 | A02 | 11898255 | G | A | downstream_gene_variant | MODIFIER | c.*4670G>A| |
S150 |
| 183518 | BAA02g22090 | A02 | 11899026 | G | A | missense_variant | MODERATE | c.473C>T|p.Thr158Ile |
S95 |
| 183519 | BAA02g22090 | A02 | 11899913 | G | A | upstream_gene_variant | MODIFIER | c.-171C>T| |
S230 |
| 183520 | BAA02g22100 | A02 | 11900173 | G | A | missense_variant | MODERATE | c.602C>T|p.Ser201Phe |
S295 |
| 183521 | BAA02g22090 | A02 | 11901500 | G | A | upstream_gene_variant | MODIFIER | c.-1758C>T| |
S204 |
| 183522 | BAA02g22090 | A02 | 11903086 | A | C | upstream_gene_variant | MODIFIER | c.-3344T>G| |
S30 |
| 183523 | BAA02g22090 | A02 | 11903261 | G | A | upstream_gene_variant | MODIFIER | c.-3519C>T| |
S12 |
| 183524 | BAA02g22090 | A02 | 11903885 | C | T | upstream_gene_variant | MODIFIER | c.-4143G>A| |
S107 |
| 183525 | BAA02g22090 | A02 | 11904194 | C | T | upstream_gene_variant | MODIFIER | c.-4452G>A| |
S135 |