Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g38630 | A06 | 25308204 | G | A | upstream_gene_variant | MODIFIER | c.-652G>A| |
S146 |
2 | BAA06g38630 | A06 | 25309059 | G | A | synonymous_variant | LOW | c.204G>A|p.Pro68Pro |
S268 |
3 | BAA06g38630 | A06 | 25309154 | C | T | missense_variant | MODERATE | c.299C>T|p.Ser100Phe |
S203 |
4 | BAA06g38630 | A06 | 25309160 | C | T | missense_variant | MODERATE | c.305C>T|p.Ala102Val |
S100 |
5 | BAA06g38630 | A06 | 25309543 | C | T | synonymous_variant | LOW | c.438C>T|p.Asp146Asp |
S6 |
6 | BAA06g38630 | A06 | 25310930 | C | T | missense_variant | MODERATE | c.1087C>T|p.Pro363Ser |
S132 S137 S215 S89 |
7 | BAA06g38630 | A06 | 25310933 | G | A | missense_variant | MODERATE | c.1090G>A|p.Ala364Thr |
S138 |
8 | BAA06g38630 | A06 | 25311044 | G | A | synonymous_variant | LOW | c.1134G>A|p.Gly378Gly |
S75 S81 |
9 | BAA06g38630 | A06 | 25311100 | G | A | missense_variant | MODERATE | c.1190G>A|p.Gly397Glu |
S263 |