Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
451 | BAA01g00320 | A01 | 161861 | G | A | missense_variant | MODERATE | c.782C>T|p.Pro261Leu |
S44 |
452 | BAA01g00320 | A01 | 161979 | C | T | intron_variant | MODIFIER | c.769-105G>A| |
S260 |
453 | BAA01g00320 | A01 | 162153 | C | T | intron_variant | MODIFIER | c.769-279G>A| |
S203 |
454 | BAA01g00320 | A01 | 162159 | C | T | intron_variant | MODIFIER | c.769-285G>A| |
S100 |
455 | BAA01g00320 | A01 | 162358 | G | A | intron_variant | MODIFIER | c.769-484C>T| |
S83 S88 |
456 | BAA01g00320 | A01 | 162410 | G | A | intron_variant | MODIFIER | c.769-536C>T| |
S244 |
457 | BAA01g00320 | A01 | 162495 | C | T | intron_variant | MODIFIER | c.769-621G>A| |
S64 |
458 | BAA01g00320 | A01 | 162560 | G | A | intron_variant | MODIFIER | c.769-686C>T| |
S75 |
459 | BAA01g00330 | A01 | 163036 | G | A | downstream_gene_variant | MODIFIER | c.*4742C>T| |
S245 |
460 | BAA01g00330 | A01 | 163177 | G | A | downstream_gene_variant | MODIFIER | c.*4601C>T| |
S185 |
461 | BAA01g00330 | A01 | 163323 | G | A | downstream_gene_variant | MODIFIER | c.*4455C>T| |
S251 |
462 | BAA01g00330 | A01 | 163765 | G | A | downstream_gene_variant | MODIFIER | c.*4013C>T| |
S162 |
463 | BAA01g00330 | A01 | 163777 | C | T | downstream_gene_variant | MODIFIER | c.*4001G>A| |
S41 |
464 | BAA01g00330 | A01 | 163909 | C | T | downstream_gene_variant | MODIFIER | c.*3869G>A| |
S140 |
465 | BAA01g00330 | A01 | 163989 | C | T | downstream_gene_variant | MODIFIER | c.*3789G>A| |
S282 |
466 | BAA01g00330 | A01 | 164105 | C | T | downstream_gene_variant | MODIFIER | c.*3673G>A| |
S192 |
467 | BAA01g00320 | A01 | 164616 | C | T | missense_variant | MODERATE | c.536G>A|p.Cys179Tyr |
S246 |
468 | BAA01g00320 | A01 | 164618 | C | T | synonymous_variant | LOW | c.534G>A|p.Ser178Ser |
S128 |
469 | BAA01g00320 | A01 | 164622 | G | A | missense_variant | MODERATE | c.530C>T|p.Pro177Leu |
S296 |
470 | BAA01g00320 | A01 | 164856 | G | A | missense_variant | MODERATE | c.296C>T|p.Pro99Leu |
S89 |
471 | BAA01g00330 | A01 | 165002 | A | G | downstream_gene_variant | MODIFIER | c.*2776T>C| |
S194 |
472 | BAA01g00330 | A01 | 165104 | C | T | downstream_gene_variant | MODIFIER | c.*2674G>A| |
S278 |
473 | BAA01g00330 | A01 | 165289 | G | T | downstream_gene_variant | MODIFIER | c.*2489C>A| |
S134 S152 S186 S192 S196 S199 S215 S47 S58 S95 |
474 | BAA01g00330 | A01 | 168087 | C | T | synonymous_variant | LOW | c.2889G>A|p.Lys963Lys |
S111 |
475 | BAA01g00330 | A01 | 168171 | C | T | stop_gained | HIGH | c.2805G>A|p.Trp935* |
S107 |