Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16390 | A01 | 7962479 | G | A | upstream_gene_variant | MODIFIER | c.-4064G>A| |
S28 |
2 | BAA01g16390 | A01 | 7962537 | C | T | upstream_gene_variant | MODIFIER | c.-4006C>T| |
S33 |
3 | BAA01g16390 | A01 | 7962933 | C | T | upstream_gene_variant | MODIFIER | c.-3610C>T| |
S20 |
4 | BAA01g16390 | A01 | 7963118 | G | A | upstream_gene_variant | MODIFIER | c.-3425G>A| |
S139 |
5 | BAA01g16390 | A01 | 7963788 | C | T | upstream_gene_variant | MODIFIER | c.-2755C>T| |
S69 |
6 | BAA01g16390 | A01 | 7964343 | G | A | upstream_gene_variant | MODIFIER | c.-2200G>A| |
S91 |
7 | BAA01g16390 | A01 | 7965760 | G | A | upstream_gene_variant | MODIFIER | c.-783G>A| |
S297 |
8 | BAA01g16390 | A01 | 7965784 | G | A | upstream_gene_variant | MODIFIER | c.-759G>A| |
S17 |
9 | BAA01g16390 | A01 | 7966771 | C | T | missense_variant | MODERATE | c.229C>T|p.Leu77Phe |
S108 |
10 | BAA01g16390 | A01 | 7969124 | C | T | missense_variant | MODERATE | c.1765C>T|p.Leu589Phe |
S111 |
11 | BAA01g16390 | A01 | 7969727 | G | A | missense_variant | MODERATE | c.2191G>A|p.Gly731Ser |
S115 |
12 | BAA01g16390 | A01 | 7970111 | C | T | missense_variant | MODERATE | c.2392C>T|p.Pro798Ser |
S135 |