Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45040 | A01 | 30035782 | G | A | missense_variant | MODERATE | c.107G>A|p.Gly36Glu |
S298 |
2 | BAA01g45040 | A01 | 30036433 | C | T | synonymous_variant | LOW | c.633C>T|p.Arg211Arg |
S233 S239 |
3 | BAA01g45040 | A01 | 30036473 | C | T | missense_variant | MODERATE | c.673C>T|p.Arg225Trp |
S35 |
4 | BAA01g45040 | A01 | 30036509 | G | A | missense_variant | MODERATE | c.709G>A|p.Val237Met |
S143 |
5 | BAA01g45040 | A01 | 30037009 | G | A | synonymous_variant | LOW | c.1119G>A|p.Lys373Lys |
S114 S119 S123 S256 |
6 | BAA01g45040 | A01 | 30037020 | G | A | missense_variant&splice_region_variant | MODERATE | c.1130G>A|p.Arg377His |
S284 |
7 | BAA01g45040 | A01 | 30037085 | G | A | splice_region_variant&intron_variant | LOW | c.1133-4G>A| |
S257 |
8 | BAA01g45040 | A01 | 30037554 | G | A | synonymous_variant | LOW | c.1536G>A|p.Arg512Arg |
S86 |
9 | BAA01g45040 | A01 | 30037672 | G | A | missense_variant | MODERATE | c.1654G>A|p.Glu552Lys |
S271 |
10 | BAA01g45040 | A01 | 30039436 | G | A | missense_variant | MODERATE | c.2924G>A|p.Arg975Lys |
S116 |
11 | BAA01g45040 | A01 | 30039488 | G | A | stop_gained | HIGH | c.2976G>A|p.Trp992* |
S135 S68 |
12 | BAA01g45040 | A01 | 30040295 | G | A | downstream_gene_variant | MODIFIER | c.*723G>A| |
S61 |
13 | BAA01g45040 | A01 | 30040496 | C | T | downstream_gene_variant | MODIFIER | c.*924C>T| |
S57 |
14 | BAA01g45040 | A01 | 30040725 | C | T | downstream_gene_variant | MODIFIER | c.*1153C>T| |
S16 |
15 | BAA01g45040 | A01 | 30041742 | C | T | downstream_gene_variant | MODIFIER | c.*2170C>T| |
S8 |