Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19050 | A08 | 15093207 | C | T | missense_variant | MODERATE | c.1558G>A|p.Val520Ile |
S245 |
2 | BAA08g19050 | A08 | 15093839 | G | A | missense_variant | MODERATE | c.1097C>T|p.Ala366Val |
S170 |
3 | BAA08g19050 | A08 | 15094423 | G | A | missense_variant | MODERATE | c.686C>T|p.Ser229Leu |
S87 |
4 | BAA08g19050 | A08 | 15095118 | G | A | missense_variant | MODERATE | c.355C>T|p.Pro119Ser |
S158 |
5 | BAA08g19050 | A08 | 15095698 | C | T | upstream_gene_variant | MODIFIER | c.-36G>A| |
S19 |
6 | BAA08g19050 | A08 | 15098167 | G | A | upstream_gene_variant | MODIFIER | c.-2505C>T| |
S61 |