Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g46660 | A06 | 29603748 | G | A | missense_variant | MODERATE | c.1375C>T|p.His459Tyr |
S197 |
2 | BAA06g46660 | A06 | 29604009 | C | T | missense_variant | MODERATE | c.1223G>A|p.Gly408Glu |
S163 |
3 | BAA06g46660 | A06 | 29604071 | C | T | synonymous_variant | LOW | c.1161G>A|p.Ala387Ala |
S288 |
4 | BAA06g46660 | A06 | 29604956 | G | A | synonymous_variant | LOW | c.447C>T|p.Arg149Arg |
S92 |
5 | BAA06g46660 | A06 | 29605463 | G | A | missense_variant | MODERATE | c.166C>T|p.Pro56Ser |
S56 |
6 | BAA06g46660 | A06 | 29608251 | G | A | upstream_gene_variant | MODIFIER | c.-2524C>T| |
S273 |
7 | BAA06g46660 | A06 | 29609117 | G | A | upstream_gene_variant | MODIFIER | c.-3390C>T| |
S81 S85 |
8 | BAA06g46660 | A06 | 29609625 | C | T | upstream_gene_variant | MODIFIER | c.-3898G>A| |
S268 |
9 | BAA06g46660 | A06 | 29610205 | G | A | upstream_gene_variant | MODIFIER | c.-4478C>T| |
S189 |
10 | BAA06g46660 | A06 | 29610383 | C | T | upstream_gene_variant | MODIFIER | c.-4656G>A| |
S235 |
11 | BAA06g46660 | A06 | 29610655 | G | A | upstream_gene_variant | MODIFIER | c.-4928C>T| |
S23 |