Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g10150 | A06 | 5091904 | C | T | downstream_gene_variant | MODIFIER | c.*1010G>A| |
S144 |
2 | BAA06g10150 | A06 | 5093273 | C | T | missense_variant | MODERATE | c.1136G>A|p.Gly379Asp |
S34 |
3 | BAA06g10150 | A06 | 5093544 | C | T | missense_variant | MODERATE | c.973G>A|p.Gly325Arg |
S46 |
4 | BAA06g10150 | A06 | 5093771 | G | A | missense_variant | MODERATE | c.842C>T|p.Ala281Val |
S217 S248 |
5 | BAA06g10150 | A06 | 5094940 | C | T | missense_variant | MODERATE | c.385G>A|p.Glu129Lys |
S242 |
6 | BAA06g10150 | A06 | 5096102 | T | C | upstream_gene_variant | MODIFIER | c.-778A>G| |
S286 |
7 | BAA06g10150 | A06 | 5098605 | C | T | upstream_gene_variant | MODIFIER | c.-3281G>A| |
S124 |
8 | BAA06g10150 | A06 | 5099036 | G | A | upstream_gene_variant | MODIFIER | c.-3712C>T| |
S85 |
9 | BAA06g10150 | A06 | 5099111 | G | A | upstream_gene_variant | MODIFIER | c.-3787C>T| |
S187 |
10 | BAA06g10150 | A06 | 5099953 | G | A | upstream_gene_variant | MODIFIER | c.-4629C>T| |
S182 |