Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g36980 | A06 | 24422667 | G | A | synonymous_variant | LOW | c.834G>A|p.Gln278Gln |
S191 |
2 | BAA06g36980 | A06 | 24423136 | C | T | missense_variant | MODERATE | c.872C>T|p.Ser291Leu |
S106 |
3 | BAA06g36980 | A06 | 24423396 | G | A | missense_variant | MODERATE | c.1132G>A|p.Glu378Lys |
S202 |
4 | BAA06g36980 | A06 | 24423937 | A | T | missense_variant | MODERATE | c.1673A>T|p.Asp558Val |
S23 |
5 | BAA06g36980 | A06 | 24424042 | G | A | missense_variant | MODERATE | c.1778G>A|p.Gly593Glu |
S122 |
6 | BAA06g36980 | A06 | 24424129 | G | A | missense_variant | MODERATE | c.1865G>A|p.Arg622His |
S206 |
7 | BAA06g36980 | A06 | 24424130 | C | A | synonymous_variant | LOW | c.1866C>A|p.Arg622Arg |
S206 |
8 | BAA06g36980 | A06 | 24424325 | G | A | downstream_gene_variant | MODIFIER | c.*192G>A| |
S262 |
9 | BAA06g36980 | A06 | 24424795 | C | T | downstream_gene_variant | MODIFIER | c.*662C>T| |
S291 |