Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g39230 | A05 | 38331958 | C | T | upstream_gene_variant | MODIFIER | c.-2327C>T| |
S298 |
2 | BAA05g39230 | A05 | 38331983 | G | A | upstream_gene_variant | MODIFIER | c.-2302G>A| |
S56 |
3 | BAA05g39230 | A05 | 38332242 | C | T | upstream_gene_variant | MODIFIER | c.-2043C>T| |
S198 |
4 | BAA05g39230 | A05 | 38332261 | C | T | upstream_gene_variant | MODIFIER | c.-2024C>T| |
S131 |
5 | BAA05g39230 | A05 | 38332573 | G | A | upstream_gene_variant | MODIFIER | c.-1712G>A| |
S281 |
6 | BAA05g39230 | A05 | 38333136 | G | A | upstream_gene_variant | MODIFIER | c.-1149G>A| |
S239 |
7 | BAA05g39230 | A05 | 38334510 | C | T | missense_variant | MODERATE | c.226C>T|p.Pro76Ser |
S72 |
8 | BAA05g39230 | A05 | 38334546 | G | A | missense_variant | MODERATE | c.262G>A|p.Asp88Asn |
S270 |
9 | BAA05g39230 | A05 | 38335392 | G | A | splice_region_variant&intron_variant | LOW | c.705-6G>A| |
S25 |
10 | BAA05g39230 | A05 | 38335682 | C | T | synonymous_variant | LOW | c.912C>T|p.Val304Val |
S249 |
11 | BAA05g39230 | A05 | 38336091 | G | A | missense_variant | MODERATE | c.1157G>A|p.Cys386Tyr |
S96 |
12 | BAA05g39230 | A05 | 38336148 | C | T | missense_variant | MODERATE | c.1214C>T|p.Pro405Leu |
S292 |
13 | BAA05g39230 | A05 | 38336525 | G | A | missense_variant | MODERATE | c.1414G>A|p.Ala472Thr |
S9 |
14 | BAA05g39230 | A05 | 38336880 | G | A | missense_variant | MODERATE | c.1594G>A|p.Gly532Arg |
S288 |
15 | BAA05g39230 | A05 | 38339920 | G | A | downstream_gene_variant | MODIFIER | c.*2954G>A| |
S111 |
16 | BAA05g39230 | A05 | 38340326 | G | A | downstream_gene_variant | MODIFIER | c.*3360G>A| |
S132 S137 S50 S89 |
17 | BAA05g39230 | A05 | 38341256 | C | T | downstream_gene_variant | MODIFIER | c.*4290C>T| |
S192 |
18 | BAA05g39230 | A05 | 38341878 | G | A | downstream_gene_variant | MODIFIER | c.*4912G>A| |
S135 |
19 | BAA05g39230 | A05 | 38341909 | G | A | downstream_gene_variant | MODIFIER | c.*4943G>A| |
S88 |