Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35670 | A02 | 30745137 | C | T | missense_variant | MODERATE | c.86C>T|p.Ser29Phe |
S301 S304 |
2 | BAA02g35670 | A02 | 30745870 | C | T | synonymous_variant | LOW | c.357C>T|p.Leu119Leu |
S257 |
3 | BAA02g35670 | A02 | 30746212 | G | A | missense_variant | MODERATE | c.616G>A|p.Asp206Asn |
S80 |
4 | BAA02g35670 | A02 | 30746811 | G | A | downstream_gene_variant | MODIFIER | c.*396G>A| |
S103 |
5 | BAA02g35670 | A02 | 30747047 | G | A | downstream_gene_variant | MODIFIER | c.*632G>A| |
S225 S73 |
6 | BAA02g35670 | A02 | 30747373 | C | T | downstream_gene_variant | MODIFIER | c.*958C>T| |
S295 |
7 | BAA02g35670 | A02 | 30747850 | C | T | downstream_gene_variant | MODIFIER | c.*1435C>T| |
S120 |
8 | BAA02g35670 | A02 | 30747962 | C | T | downstream_gene_variant | MODIFIER | c.*1547C>T| |
S226 |
9 | BAA02g35670 | A02 | 30748577 | C | T | downstream_gene_variant | MODIFIER | c.*2162C>T| |
S168 S278 |
10 | BAA02g35670 | A02 | 30749598 | T | A | downstream_gene_variant | MODIFIER | c.*3183T>A| |
S124 S126 S128 S131 S190 S223 S255 S284 S286 S57 S59 |
11 | BAA02g35670 | A02 | 30750263 | C | T | downstream_gene_variant | MODIFIER | c.*3848C>T| |
S6 |
12 | BAA02g35670 | A02 | 30750365 | C | T | downstream_gene_variant | MODIFIER | c.*3950C>T| |
S2 |