Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g14180 | A03 | 5865444 | C | T | missense_variant | MODERATE | c.986C>T|p.Pro329Leu |
S83 S88 |
2 | BAA03g14180 | A03 | 5865507 | C | T | missense_variant | MODERATE | c.1049C>T|p.Pro350Leu |
S159 S243 |
3 | BAA03g14180 | A03 | 5865595 | C | T | synonymous_variant | LOW | c.1137C>T|p.Ile379Ile |
S73 S91 |
4 | BAA03g14180 | A03 | 5865625 | G | A | synonymous_variant | LOW | c.1167G>A|p.Lys389Lys |
S235 |
5 | BAA03g14180 | A03 | 5865935 | G | A | missense_variant | MODERATE | c.1477G>A|p.Val493Met |
S122 |
6 | BAA03g14180 | A03 | 5866072 | G | A | synonymous_variant | LOW | c.1614G>A|p.Lys538Lys |
S149 |
7 | BAA03g14180 | A03 | 5869123 | C | T | intron_variant | MODIFIER | c.2091+2574C>T| |
S65 |
8 | BAA03g14180 | A03 | 5870956 | C | T | intron_variant | MODIFIER | c.2091+4407C>T| |
S107 |
9 | BAA03g14180 | A03 | 5872291 | G | A | intron_variant | MODIFIER | c.2091+5742G>A| |
S130 |
10 | BAA03g14180 | A03 | 5872693 | G | A | intron_variant | MODIFIER | c.2091+6144G>A| |
S294 |
11 | BAA03g14180 | A03 | 5873800 | G | A | intron_variant | MODIFIER | c.2092-5701G>A| |
S119 |
12 | BAA03g14180 | A03 | 5874582 | G | A | intron_variant | MODIFIER | c.2092-4919G>A| |
S229 |
13 | BAA03g14180 | A03 | 5874973 | C | T | intron_variant | MODIFIER | c.2092-4528C>T| |
S132 S137 |