Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g69630 | A09 | 62091629 | G | A | upstream_gene_variant | MODIFIER | c.-1500G>A| |
S273 |
2 | BAA09g69630 | A09 | 62093342 | A | C | missense_variant | MODERATE | c.214A>C|p.Lys72Gln |
S245 |
3 | BAA09g69630 | A09 | 62093454 | G | A | missense_variant | MODERATE | c.326G>A|p.Arg109Lys |
S12 |
4 | BAA09g69630 | A09 | 62093928 | C | T | missense_variant | MODERATE | c.619C>T|p.Leu207Phe |
S198 |
5 | BAA09g69630 | A09 | 62094332 | C | T | missense_variant | MODERATE | c.812C>T|p.Pro271Leu |
S275 |
6 | BAA09g69630 | A09 | 62094347 | G | A | missense_variant | MODERATE | c.827G>A|p.Arg276Gln |
S233 |
7 | BAA09g69630 | A09 | 62099345 | G | A | downstream_gene_variant | MODIFIER | c.*4175G>A| |
S148 S30 S31 |
8 | BAA09g69630 | A09 | 62099537 | G | A | downstream_gene_variant | MODIFIER | c.*4367G>A| |
S188 |
9 | BAA09g69630 | A09 | 62099871 | C | T | downstream_gene_variant | MODIFIER | c.*4701C>T| |
S54 |