Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g14240 | A03 | 5899217 | G | A | missense_variant | MODERATE | c.3512C>T|p.Pro1171Leu |
S13 |
2 | BAA03g14240 | A03 | 5899850 | C | T | synonymous_variant | LOW | c.3258G>A|p.Glu1086Glu |
S32 |
3 | BAA03g14240 | A03 | 5900134 | C | T | missense_variant | MODERATE | c.3088G>A|p.Val1030Ile |
S142 |
4 | BAA03g14240 | A03 | 5900179 | C | T | missense_variant | MODERATE | c.3043G>A|p.Glu1015Lys |
S8 |
5 | BAA03g14240 | A03 | 5900929 | C | T | missense_variant | MODERATE | c.2293G>A|p.Val765Met |
S19 |
6 | BAA03g14240 | A03 | 5901154 | G | A | missense_variant | MODERATE | c.2068C>T|p.Pro690Ser |
S104 S52 |
7 | BAA03g14240 | A03 | 5901188 | C | T | synonymous_variant | LOW | c.2034G>A|p.Glu678Glu |
S247 |
8 | BAA03g14240 | A03 | 5901785 | C | T | synonymous_variant | LOW | c.1437G>A|p.Arg479Arg |
S123 |
9 | BAA03g14240 | A03 | 5902020 | C | T | missense_variant | MODERATE | c.1202G>A|p.Gly401Glu |
S46 |
10 | BAA03g14240 | A03 | 5902655 | C | T | synonymous_variant | LOW | c.567G>A|p.Gln189Gln |
S87 |
11 | BAA03g14240 | A03 | 5902671 | G | A | missense_variant | MODERATE | c.551C>T|p.Ser184Phe |
S120 |
12 | BAA03g14240 | A03 | 5902820 | G | A | synonymous_variant | LOW | c.402C>T|p.His134His |
S167 |
13 | BAA03g14240 | A03 | 5904565 | G | A | upstream_gene_variant | MODIFIER | c.-1064C>T| |
S138 |
14 | BAA03g14240 | A03 | 5904999 | C | T | upstream_gene_variant | MODIFIER | c.-1498G>A| |
S260 |
15 | BAA03g14240 | A03 | 5906513 | C | T | upstream_gene_variant | MODIFIER | c.-3012G>A| |
S15 S3 |