Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g55960 | A09 | 55860102 | C | T | synonymous_variant | LOW | c.1293G>A|p.Val431Val |
S83 S88 |
2 | BAA09g55960 | A09 | 55860146 | C | T | missense_variant | MODERATE | c.1249G>A|p.Asp417Asn |
S100 |
3 | BAA09g55960 | A09 | 55860178 | C | T | missense_variant | MODERATE | c.1217G>A|p.Gly406Asp |
S168 |
4 | BAA09g55960 | A09 | 55860627 | G | A | synonymous_variant | LOW | c.768C>T|p.Pro256Pro |
S55 |
5 | BAA09g55960 | A09 | 55861135 | G | A | missense_variant | MODERATE | c.260C>T|p.Ser87Phe |
S233 |
6 | BAA09g55960 | A09 | 55861390 | C | T | missense_variant | MODERATE | c.5G>A|p.Gly2Asp |
S294 |
7 | BAA09g55960 | A09 | 55863069 | G | A | upstream_gene_variant | MODIFIER | c.-1675C>T| |
S177 |
8 | BAA09g55960 | A09 | 55863258 | G | A | upstream_gene_variant | MODIFIER | c.-1864C>T| |
S292 |
9 | BAA09g55960 | A09 | 55864250 | G | A | upstream_gene_variant | MODIFIER | c.-2856C>T| |
S115 |
10 | BAA09g55960 | A09 | 55864508 | G | A | upstream_gene_variant | MODIFIER | c.-3114C>T| |
S2 |
11 | BAA09g55960 | A09 | 55865682 | G | A | upstream_gene_variant | MODIFIER | c.-4288C>T| |
S144 |