Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g08670 | A04 | 5986227 | G | A | upstream_gene_variant | MODIFIER | c.-3278G>A| |
S271 |
2 | BAA04g08670 | A04 | 5988142 | G | A | upstream_gene_variant | MODIFIER | c.-1363G>A| |
S69 |
3 | BAA04g08670 | A04 | 5988418 | G | A | upstream_gene_variant | MODIFIER | c.-1087G>A| |
S19 |
4 | BAA04g08670 | A04 | 5988435 | C | A | upstream_gene_variant | MODIFIER | c.-1070C>A| |
S138 S23 |
5 | BAA04g08670 | A04 | 5988467 | G | A | upstream_gene_variant | MODIFIER | c.-1038G>A| |
S108 |
6 | BAA04g08670 | A04 | 5989863 | G | A | missense_variant | MODERATE | c.199G>A|p.Gly67Arg |
S288 |
7 | BAA04g08670 | A04 | 5990133 | C | T | missense_variant | MODERATE | c.391C>T|p.Pro131Ser |
S173 |
8 | BAA04g08670 | A04 | 5991031 | C | T | missense_variant&splice_region_variant | MODERATE | c.851C>T|p.Thr284Ile |
S73 |
9 | BAA04g08670 | A04 | 5991899 | C | T | synonymous_variant | LOW | c.1176C>T|p.Phe392Phe |
S92 |
10 | BAA04g08670 | A04 | 5992464 | C | T | missense_variant | MODERATE | c.1348C>T|p.Leu450Phe |
S265 |
11 | BAA04g08670 | A04 | 5992483 | C | T | missense_variant | MODERATE | c.1367C>T|p.Thr456Ile |
S63 |
12 | BAA04g08670 | A04 | 5994125 | G | A | downstream_gene_variant | MODIFIER | c.*1376G>A| |
S19 |
13 | BAA04g08670 | A04 | 5994547 | G | A | downstream_gene_variant | MODIFIER | c.*1798G>A| |
S171 |
14 | BAA04g08670 | A04 | 5996291 | G | A | downstream_gene_variant | MODIFIER | c.*3542G>A| |
S144 |
15 | BAA04g08670 | A04 | 5996515 | C | T | downstream_gene_variant | MODIFIER | c.*3766C>T| |
S116 |
16 | BAA04g08670 | A04 | 5996951 | C | T | downstream_gene_variant | MODIFIER | c.*4202C>T| |
S169 S225 |