Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g25060 | A07 | 28027982 | G | A | upstream_gene_variant | MODIFIER | c.-3042G>A| |
S209 |
2 | BAA07g25060 | A07 | 28032287 | C | T | missense_variant | MODERATE | c.208C>T|p.Pro70Ser |
S192 |
3 | BAA07g25060 | A07 | 28032398 | G | A | missense_variant | MODERATE | c.319G>A|p.Glu107Lys |
S163 |
4 | BAA07g25060 | A07 | 28032848 | C | T | synonymous_variant | LOW | c.769C>T|p.Leu257Leu |
S23 |
5 | BAA07g25060 | A07 | 28033833 | C | T | missense_variant | MODERATE | c.1754C>T|p.Ser585Phe |
S103 |
6 | BAA07g25060 | A07 | 28035010 | G | A | missense_variant | MODERATE | c.2563G>A|p.Ala855Thr |
S276 |
7 | BAA07g25060 | A07 | 28035573 | G | A | missense_variant | MODERATE | c.2695G>A|p.Ala899Thr |
S128 |
8 | BAA07g25060 | A07 | 28036330 | G | A | synonymous_variant | LOW | c.3222G>A|p.Val1074Val |
S170 |
9 | BAA07g25060 | A07 | 28036840 | C | T | missense_variant | MODERATE | c.3652C>T|p.His1218Tyr |
S159 S243 |
10 | BAA07g25060 | A07 | 28036887 | G | A | synonymous_variant | LOW | c.3699G>A|p.Glu1233Glu |
S210 S225 |