Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18660 | A08 | 14902947 | G | A | missense_variant | MODERATE | c.872C>T|p.Thr291Ile |
S162 |
2 | BAA08g18660 | A08 | 14903603 | G | A | synonymous_variant | LOW | c.480C>T|p.Phe160Phe |
S151 S263 |
3 | BAA08g18660 | A08 | 14904170 | G | A | synonymous_variant | LOW | c.60C>T|p.Ser20Ser |
S224 |
4 | BAA08g18660 | A08 | 14904794 | G | A | upstream_gene_variant | MODIFIER | c.-565C>T| |
S269 |
5 | BAA08g18660 | A08 | 14905990 | C | T | upstream_gene_variant | MODIFIER | c.-1761G>A| |
S305 |
6 | BAA08g18660 | A08 | 14907319 | C | T | upstream_gene_variant | MODIFIER | c.-3090G>A| |
S71 |
7 | BAA08g18660 | A08 | 14907328 | G | A | upstream_gene_variant | MODIFIER | c.-3099C>T| |
S182 |
8 | BAA08g18660 | A08 | 14907593 | C | T | upstream_gene_variant | MODIFIER | c.-3364G>A| |
S207 |