Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g13590 | A06 | 6739374 | G | A | upstream_gene_variant | MODIFIER | c.-4820G>A| |
S32 |
2 | BAA06g13590 | A06 | 6739725 | G | A | upstream_gene_variant | MODIFIER | c.-4469G>A| |
S292 |
3 | BAA06g13590 | A06 | 6740025 | T | C | upstream_gene_variant | MODIFIER | c.-4169T>C| |
S235 |
4 | BAA06g13590 | A06 | 6740055 | G | A | upstream_gene_variant | MODIFIER | c.-4139G>A| |
S63 |
5 | BAA06g13590 | A06 | 6743783 | C | T | upstream_gene_variant | MODIFIER | c.-411C>T| |
S150 |
6 | BAA06g13590 | A06 | 6743987 | C | T | upstream_gene_variant | MODIFIER | c.-207C>T| |
S98 |
7 | BAA06g13590 | A06 | 6744107 | C | T | upstream_gene_variant | MODIFIER | c.-87C>T| |
S36 |
8 | BAA06g13590 | A06 | 6745256 | G | A | missense_variant | MODERATE | c.526G>A|p.Val176Met |
S25 |
9 | BAA06g13590 | A06 | 6746095 | C | T | missense_variant | MODERATE | c.1168C>T|p.Leu390Phe |
S278 |