| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 151651 | BAA02g00320 | A02 | 185411 | C | T | downstream_gene_variant | MODIFIER | c.*2791G>A| |
S13 S88 |
| 151652 | BAA02g00320 | A02 | 185462 | C | T | downstream_gene_variant | MODIFIER | c.*2740G>A| |
S234 |
| 151653 | BAA02g00320 | A02 | 187161 | C | T | downstream_gene_variant | MODIFIER | c.*1041G>A| |
S243 S299 |
| 151654 | BAA02g00320 | A02 | 187208 | C | T | downstream_gene_variant | MODIFIER | c.*994G>A| |
S241 |
| 151655 | BAA02g00320 | A02 | 187429 | C | T | downstream_gene_variant | MODIFIER | c.*773G>A| |
S124 |
| 151656 | BAA02g00320 | A02 | 188208 | C | T | stop_gained | HIGH | c.789G>A|p.Trp263* |
S242 |
| 151657 | BAA02g00330 | A02 | 188814 | G | A | downstream_gene_variant | MODIFIER | c.*3685C>T| |
S149 |
| 151658 | BAA02g00320 | A02 | 189099 | G | A | synonymous_variant | LOW | c.288C>T|p.Tyr96Tyr |
S87 |
| 151659 | BAA02g00320 | A02 | 189218 | C | T | missense_variant | MODERATE | c.169G>A|p.Gly57Arg |
S183 S198 |
| 151660 | BAA02g00320 | A02 | 192188 | G | A | upstream_gene_variant | MODIFIER | c.-2802C>T| |
S165 |
| 151661 | BAA02g00330 | A02 | 192941 | C | T | missense_variant | MODERATE | c.1447G>A|p.Asp483Asn |
S138 |
| 151662 | BAA02g00330 | A02 | 193168 | G | A | missense_variant | MODERATE | c.1220C>T|p.Thr407Ile |
S107 |
| 151663 | BAA02g00330 | A02 | 193505 | C | T | missense_variant | MODERATE | c.883G>A|p.Asp295Asn |
S135 |
| 151664 | BAA02g00330 | A02 | 194937 | C | T | upstream_gene_variant | MODIFIER | c.-63G>A| |
S278 S42 |
| 151665 | BAA02g00330 | A02 | 198306 | G | A | upstream_gene_variant | MODIFIER | c.-3432C>T| |
S190 |
| 151666 | BAA02g00340 | A02 | 198737 | G | A | missense_variant | MODERATE | c.410C>T|p.Ser137Leu |
S296 |
| 151667 | BAA02g00350 | A02 | 201266 | G | A | synonymous_variant | LOW | c.339G>A|p.Leu113Leu |
S256 |
| 151668 | BAA02g00350 | A02 | 201383 | G | A | synonymous_variant | LOW | c.456G>A|p.Glu152Glu |
S136 |
| 151669 | BAA02g00350 | A02 | 201415 | G | A | missense_variant | MODERATE | c.488G>A|p.Arg163Lys |
S76 |
| 151670 | BAA02g00350 | A02 | 201980 | G | A | splice_donor_variant&intron_variant | HIGH | c.797+1G>A| |
S57 |
| 151671 | BAA02g00350 | A02 | 202666 | G | A | synonymous_variant | LOW | c.1323G>A|p.Pro441Pro |
S169 |
| 151672 | BAA02g00340 | A02 | 203585 | G | A | upstream_gene_variant | MODIFIER | c.-4439C>T| |
S155 S211 |
| 151673 | BAA02g00340 | A02 | 203990 | C | T | upstream_gene_variant | MODIFIER | c.-4844G>A| |
S55 |
| 151674 | BAA02g00340 | A02 | 204037 | C | T | upstream_gene_variant | MODIFIER | c.-4891G>A| |
S242 S38 |
| 151675 | BAA02g00350 | A02 | 204442 | C | T | downstream_gene_variant | MODIFIER | c.*1111C>T| |
S159 |