Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g19070 | A05 | 11130055 | C | T | upstream_gene_variant | MODIFIER | c.-1067C>T| |
S12 |
2 | BAA05g19070 | A05 | 11130356 | G | A | upstream_gene_variant | MODIFIER | c.-766G>A| |
|
3 | BAA05g19070 | A05 | 11130852 | C | T | upstream_gene_variant | MODIFIER | c.-270C>T| |
S99 |
4 | BAA05g19070 | A05 | 11130930 | G | A | upstream_gene_variant | MODIFIER | c.-192G>A| |
S156 |
5 | BAA05g19070 | A05 | 11130983 | C | T | upstream_gene_variant | MODIFIER | c.-139C>T| |
S5 |
6 | BAA05g19070 | A05 | 11131203 | G | A | missense_variant | MODERATE | c.82G>A|p.Glu28Lys |
S170 |
7 | BAA05g19070 | A05 | 11131226 | C | T | synonymous_variant | LOW | c.105C>T|p.Val35Val |
S142 |
8 | BAA05g19070 | A05 | 11134188 | G | A | missense_variant | MODERATE | c.487G>A|p.Ala163Thr |
S14 |
9 | BAA05g19070 | A05 | 11134281 | C | T | missense_variant | MODERATE | c.580C>T|p.Pro194Ser |
S233 |
10 | BAA05g19070 | A05 | 11134293 | C | T | missense_variant | MODERATE | c.592C>T|p.Pro198Ser |
S255 |
11 | BAA05g19070 | A05 | 11134463 | C | T | synonymous_variant | LOW | c.762C>T|p.Arg254Arg |
S136 |
12 | BAA05g19070 | A05 | 11137508 | G | A | downstream_gene_variant | MODIFIER | c.*1995G>A| |
S282 |
13 | BAA05g19070 | A05 | 11139397 | A | C | downstream_gene_variant | MODIFIER | c.*3884A>C| |
S117 S118 S122 S129 S176 S177 S185 S192 S196 S243 S257 S52 |
14 | BAA05g19070 | A05 | 11139474 | C | T | downstream_gene_variant | MODIFIER | c.*3961C>T| |
S111 |
15 | BAA05g19070 | A05 | 11140328 | C | T | downstream_gene_variant | MODIFIER | c.*4815C>T| |
S165 |