Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g36030 | A02 | 30993948 | C | T | upstream_gene_variant | MODIFIER | c.-3162C>T| |
S233 |
2 | BAA02g36030 | A02 | 30994509 | G | A | upstream_gene_variant | MODIFIER | c.-2601G>A| |
S306 S308 |
3 | BAA02g36030 | A02 | 30997248 | C | T | missense_variant | MODERATE | c.139C>T|p.Leu47Phe |
S179 |
4 | BAA02g36030 | A02 | 30997511 | C | T | synonymous_variant | LOW | c.402C>T|p.Tyr134Tyr |
S162 |
5 | BAA02g36030 | A02 | 30997668 | C | T | missense_variant | MODERATE | c.559C>T|p.Leu187Phe |
S15 S3 |
6 | BAA02g36030 | A02 | 30998505 | G | A | missense_variant | MODERATE | c.1066G>A|p.Gly356Ser |
S35 |
7 | BAA02g36030 | A02 | 30998531 | G | A | synonymous_variant | LOW | c.1092G>A|p.Gly364Gly |
S203 |
8 | BAA02g36030 | A02 | 30999184 | G | A | downstream_gene_variant | MODIFIER | c.*560G>A| |
S279 |
9 | BAA02g36030 | A02 | 31000655 | C | T | downstream_gene_variant | MODIFIER | c.*2031C>T| |
S159 S188 S243 S276 S298 S299 |
10 | BAA02g36030 | A02 | 31000891 | C | T | downstream_gene_variant | MODIFIER | c.*2267C>T| |
S98 |