Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40920 | A02 | 34310306 | C | T | upstream_gene_variant | MODIFIER | c.-4705C>T| |
S120 |
2 | BAA02g40920 | A02 | 34311326 | C | T | upstream_gene_variant | MODIFIER | c.-3685C>T| |
S48 |
3 | BAA02g40920 | A02 | 34311586 | C | T | upstream_gene_variant | MODIFIER | c.-3425C>T| |
S249 |
4 | BAA02g40920 | A02 | 34315252 | C | T | missense_variant | MODERATE | c.242C>T|p.Thr81Ile |
S120 |
5 | BAA02g40920 | A02 | 34315514 | C | T | synonymous_variant | LOW | c.504C>T|p.Cys168Cys |
S13 |
6 | BAA02g40920 | A02 | 34315803 | G | A | missense_variant | MODERATE | c.664G>A|p.Asp222Asn |
S251 S267 |
7 | BAA02g40920 | A02 | 34316143 | G | A | missense_variant | MODERATE | c.1004G>A|p.Gly335Glu |
S286 |
8 | BAA02g40920 | A02 | 34316615 | C | T | synonymous_variant | LOW | c.1380C>T|p.Arg460Arg |
S171 |
9 | BAA02g40920 | A02 | 34316653 | G | A | missense_variant | MODERATE | c.1418G>A|p.Cys473Tyr |
S69 |
10 | BAA02g40920 | A02 | 34316763 | G | A | missense_variant | MODERATE | c.1528G>A|p.Gly510Arg |
S263 |
11 | BAA02g40920 | A02 | 34316956 | C | T | missense_variant | MODERATE | c.1721C>T|p.Thr574Ile |
S63 |
12 | BAA02g40920 | A02 | 34317230 | G | A | synonymous_variant | LOW | c.1995G>A|p.Gly665Gly |
S71 |
13 | BAA02g40920 | A02 | 34318888 | G | A | downstream_gene_variant | MODIFIER | c.*1595G>A| |
S282 |