| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 167551 | BAA02g13220 | A02 | 5999612 | G | A | missense_variant | MODERATE | c.166C>T|p.Pro56Ser |
S125 |
| 167552 | BAA02g13220 | A02 | 6000205 | C | T | upstream_gene_variant | MODIFIER | c.-428G>A| |
S55 |
| 167553 | BAA02g13220 | A02 | 6001029 | C | T | upstream_gene_variant | MODIFIER | c.-1252G>A| |
S299 |
| 167554 | BAA02g13230 | A02 | 6003041 | C | T | synonymous_variant | LOW | c.99C>T|p.Leu33Leu |
S277 |
| 167555 | BAA02g13230 | A02 | 6003084 | G | A | missense_variant | MODERATE | c.142G>A|p.Ala48Thr |
S105 S106 |
| 167556 | BAA02g13220 | A02 | 6003480 | G | A | upstream_gene_variant | MODIFIER | c.-3703C>T| |
S148 S30 S31 |
| 167557 | BAA02g13220 | A02 | 6003511 | G | A | upstream_gene_variant | MODIFIER | c.-3734C>T| |
S295 |
| 167558 | BAA02g13230 | A02 | 6003799 | C | T | missense_variant | MODERATE | c.470C>T|p.Ala157Val |
S158 |
| 167559 | BAA02g13230 | A02 | 6003801 | G | A | missense_variant | MODERATE | c.472G>A|p.Ala158Thr |
S191 |
| 167560 | BAA02g13230 | A02 | 6003815 | G | A | synonymous_variant | LOW | c.486G>A|p.Gly162Gly |
S62 |
| 167561 | BAA02g13230 | A02 | 6004192 | C | T | splice_region_variant&intron_variant | LOW | c.715+6C>T| |
S226 |
| 167562 | BAA02g13220 | A02 | 6004420 | C | T | upstream_gene_variant | MODIFIER | c.-4643G>A| |
S139 |
| 167563 | BAA02g13230 | A02 | 6005936 | G | A | downstream_gene_variant | MODIFIER | c.*57G>A| |
S205 |
| 167564 | BAA02g13230 | A02 | 6008382 | G | A | downstream_gene_variant | MODIFIER | c.*2503G>A| |
S296 |
| 167565 | BAA02g13230 | A02 | 6010241 | G | A | downstream_gene_variant | MODIFIER | c.*4362G>A| |
S296 |
| 167566 | BAA02g13240 | A02 | 6010908 | C | T | upstream_gene_variant | MODIFIER | c.-4900C>T| |
S293 |
| 167567 | BAA02g13240 | A02 | 6012517 | G | A | upstream_gene_variant | MODIFIER | c.-3291G>A| |
S184 |
| 167568 | BAA02g13240 | A02 | 6012967 | C | T | upstream_gene_variant | MODIFIER | c.-2841C>T| |
S201 |
| 167569 | BAA02g13240 | A02 | 6013279 | G | A | upstream_gene_variant | MODIFIER | c.-2529G>A| |
S126 |
| 167570 | BAA02g13240 | A02 | 6013453 | G | A | upstream_gene_variant | MODIFIER | c.-2355G>A| |
S288 |
| 167571 | BAA02g13240 | A02 | 6013982 | C | T | upstream_gene_variant | MODIFIER | c.-1826C>T| |
S242 |
| 167572 | BAA02g13240 | A02 | 6015187 | C | T | upstream_gene_variant | MODIFIER | c.-621C>T| |
S5 |
| 167573 | BAA02g13250 | A02 | 6015860 | G | A | downstream_gene_variant | MODIFIER | c.*3384C>T| |
S205 |
| 167574 | BAA02g13250 | A02 | 6016435 | C | T | downstream_gene_variant | MODIFIER | c.*2809G>A| |
S211 S227 |
| 167575 | BAA02g13240 | A02 | 6017353 | C | T | missense_variant | MODERATE | c.743C>T|p.Thr248Ile |
S283 |