Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01130 | A09 | 812816 | C | T | upstream_gene_variant | MODIFIER | c.-4005C>T| |
S270 |
2 | BAA09g01130 | A09 | 814441 | G | A | upstream_gene_variant | MODIFIER | c.-2380G>A| |
S164 |
3 | BAA09g01130 | A09 | 815335 | G | A | upstream_gene_variant | MODIFIER | c.-1486G>A| |
S97 |
4 | BAA09g01130 | A09 | 815380 | C | T | upstream_gene_variant | MODIFIER | c.-1441C>T| |
S161 |
5 | BAA09g01130 | A09 | 817367 | C | T | intron_variant | MODIFIER | c.249-145C>T| |
S286 |
6 | BAA09g01130 | A09 | 817913 | G | A | missense_variant | MODERATE | c.554G>A|p.Cys185Tyr |
S202 |
7 | BAA09g01130 | A09 | 818494 | C | T | missense_variant | MODERATE | c.850C>T|p.Pro284Ser |
S144 |
8 | BAA09g01130 | A09 | 818959 | C | T | downstream_gene_variant | MODIFIER | c.*134C>T| |
S118 |
9 | BAA09g01130 | A09 | 820612 | G | A | downstream_gene_variant | MODIFIER | c.*1787G>A| |
S23 |
10 | BAA09g01130 | A09 | 821426 | C | T | downstream_gene_variant | MODIFIER | c.*2601C>T| |
S161 |