Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g43660 | A05 | 41013060 | G | A | upstream_gene_variant | MODIFIER | c.-4709G>A| |
S117 |
2 | BAA05g43660 | A05 | 41014215 | G | A | upstream_gene_variant | MODIFIER | c.-3554G>A| |
S275 |
3 | BAA05g43660 | A05 | 41018638 | G | A | missense_variant | MODERATE | c.870G>A|p.Met290Ile |
S218 S269 |
4 | BAA05g43660 | A05 | 41019569 | G | C | missense_variant | MODERATE | c.1757G>C|p.Cys586Ser |
S143 |
5 | BAA05g43660 | A05 | 41019745 | G | A | missense_variant | MODERATE | c.1933G>A|p.Gly645Arg |
S48 |
6 | BAA05g43660 | A05 | 41019950 | G | A | missense_variant | MODERATE | c.2138G>A|p.Gly713Glu |
S295 |
7 | BAA05g43660 | A05 | 41020017 | C | T | synonymous_variant | LOW | c.2205C>T|p.Phe735Phe |
S139 |
8 | BAA05g43660 | A05 | 41020225 | G | A | missense_variant | MODERATE | c.2413G>A|p.Val805Ile |
S150 |
9 | BAA05g43660 | A05 | 41020671 | G | A | synonymous_variant | LOW | c.2859G>A|p.Ala953Ala |
S251 |
10 | BAA05g43660 | A05 | 41023454 | C | T | downstream_gene_variant | MODIFIER | c.*462C>T| |
S71 |
11 | BAA05g43660 | A05 | 41023469 | C | T | downstream_gene_variant | MODIFIER | c.*477C>T| |
S7 |