Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g52680 | A09 | 54300537 | C | T | missense_variant | MODERATE | c.352C>T|p.Leu118Phe |
S301 S304 |
2 | BAA09g52680 | A09 | 54300793 | G | A | missense_variant | MODERATE | c.608G>A|p.Gly203Asp |
S185 |
3 | BAA09g52680 | A09 | 54300834 | G | A | missense_variant | MODERATE | c.649G>A|p.Asp217Asn |
S92 |
4 | BAA09g52680 | A09 | 54301245 | G | A | missense_variant | MODERATE | c.1060G>A|p.Asp354Asn |
S187 |
5 | BAA09g52680 | A09 | 54301314 | G | A | missense_variant | MODERATE | c.1129G>A|p.Glu377Lys |
S200 |
6 | BAA09g52680 | A09 | 54301541 | G | A | synonymous_variant | LOW | c.1356G>A|p.Glu452Glu |
S178 |
7 | BAA09g52680 | A09 | 54305071 | G | A | downstream_gene_variant | MODIFIER | c.*3002G>A| |
S11 |
8 | BAA09g52680 | A09 | 54305219 | C | T | downstream_gene_variant | MODIFIER | c.*3150C>T| |
S119 |
9 | BAA09g52680 | A09 | 54306448 | G | A | downstream_gene_variant | MODIFIER | c.*4379G>A| |
S12 |
10 | BAA09g52680 | A09 | 54306551 | G | A | downstream_gene_variant | MODIFIER | c.*4482G>A| |
S116 |