Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g09720 | A09 | 5390521 | C | T | missense_variant | MODERATE | c.2023G>A|p.Glu675Lys |
S111 |
2 | BAA09g09720 | A09 | 5390854 | C | T | missense_variant | MODERATE | c.1690G>A|p.Ala564Thr |
S282 |
3 | BAA09g09720 | A09 | 5391117 | G | A | missense_variant | MODERATE | c.1427C>T|p.Ala476Val |
S80 |
4 | BAA09g09720 | A09 | 5391581 | C | T | synonymous_variant | LOW | c.963G>A|p.Leu321Leu |
S152 |
5 | BAA09g09720 | A09 | 5391891 | G | A | missense_variant | MODERATE | c.653C>T|p.Ser218Phe |
S199 |
6 | BAA09g09720 | A09 | 5392003 | G | A | synonymous_variant | LOW | c.541C>T|p.Leu181Leu |
S9 |
7 | BAA09g09720 | A09 | 5392788 | G | A | missense_variant | MODERATE | c.95C>T|p.Ser32Phe |
S202 |
8 | BAA09g09720 | A09 | 5393243 | C | T | upstream_gene_variant | MODIFIER | c.-261G>A| |
S186 |
9 | BAA09g09720 | A09 | 5395351 | G | A | upstream_gene_variant | MODIFIER | c.-2369C>T| |
S243 |