Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g10020 | A08 | 9113467 | G | A | missense_variant | MODERATE | c.1277C>T|p.Ala426Val |
S25 |
2 | BAA08g10020 | A08 | 9116091 | G | A | missense_variant | MODERATE | c.299C>T|p.Ser100Phe |
S288 |
3 | BAA08g10020 | A08 | 9116097 | C | A | missense_variant | MODERATE | c.293G>T|p.Trp98Leu |
S261 |
4 | BAA08g10020 | A08 | 9116524 | C | T | missense_variant | MODERATE | c.31G>A|p.Gly11Ser |
S256 |
5 | BAA08g10020 | A08 | 9116817 | G | A | upstream_gene_variant | MODIFIER | c.-263C>T| |
S35 |
6 | BAA08g10020 | A08 | 9117144 | C | T | upstream_gene_variant | MODIFIER | c.-590G>A| |
S209 |
7 | BAA08g10020 | A08 | 9118841 | C | T | upstream_gene_variant | MODIFIER | c.-2287G>A| |
S47 |
8 | BAA08g10020 | A08 | 9120929 | C | T | upstream_gene_variant | MODIFIER | c.-4375G>A| |
S17 |
9 | BAA08g10020 | A08 | 9120957 | G | A | upstream_gene_variant | MODIFIER | c.-4403C>T| |
S151 |
10 | BAA08g10020 | A08 | 9121447 | G | A | upstream_gene_variant | MODIFIER | c.-4893C>T| |
S246 |