Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g58530 | A03 | 29250894 | G | A | upstream_gene_variant | MODIFIER | c.-1245G>A| |
S217 |
2 | BAA03g58530 | A03 | 29251786 | G | A | upstream_gene_variant | MODIFIER | c.-353G>A| |
S217 S248 |
3 | BAA03g58530 | A03 | 29252334 | G | A | missense_variant | MODERATE | c.196G>A|p.Val66Ile |
S247 |
4 | BAA03g58530 | A03 | 29252520 | G | A | missense_variant | MODERATE | c.382G>A|p.Ala128Thr |
S257 |
5 | BAA03g58530 | A03 | 29253199 | G | A | missense_variant | MODERATE | c.1061G>A|p.Ser354Asn |
S190 |
6 | BAA03g58530 | A03 | 29253219 | G | T | missense_variant | MODERATE | c.1081G>T|p.Val361Phe |
S203 |
7 | BAA03g58530 | A03 | 29253239 | G | A | synonymous_variant | LOW | c.1101G>A|p.Val367Val |
S95 |
8 | BAA03g58530 | A03 | 29253299 | G | A | synonymous_variant | LOW | c.1161G>A|p.Leu387Leu |
S256 |
9 | BAA03g58530 | A03 | 29254129 | C | T | downstream_gene_variant | MODIFIER | c.*677C>T| |
S16 |
10 | BAA03g58530 | A03 | 29254456 | C | T | downstream_gene_variant | MODIFIER | c.*1004C>T| |
S97 |
11 | BAA03g58530 | A03 | 29254752 | G | A | downstream_gene_variant | MODIFIER | c.*1300G>A| |
S286 |
12 | BAA03g58530 | A03 | 29254957 | G | A | downstream_gene_variant | MODIFIER | c.*1505G>A| |
S134 |
13 | BAA03g58530 | A03 | 29255777 | C | T | downstream_gene_variant | MODIFIER | c.*2325C>T| |
S118 |
14 | BAA03g58530 | A03 | 29256686 | C | T | downstream_gene_variant | MODIFIER | c.*3234C>T| |
S30 S31 |
15 | BAA03g58530 | A03 | 29256718 | C | T | downstream_gene_variant | MODIFIER | c.*3266C>T| |
S187 |
16 | BAA03g58530 | A03 | 29256910 | G | A | downstream_gene_variant | MODIFIER | c.*3458G>A| |
S298 |