Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g08430 | A01 | 3720880 | G | A | missense_variant | MODERATE | c.221G>A|p.Arg74Lys |
S228 |
2 | BAA01g08430 | A01 | 3722019 | C | T | missense_variant | MODERATE | c.1189C>T|p.Leu397Phe |
S211 S227 |
3 | BAA01g08430 | A01 | 3722060 | C | T | synonymous_variant | LOW | c.1230C>T|p.Leu410Leu |
S139 |
4 | BAA01g08430 | A01 | 3722608 | G | A | splice_region_variant&intron_variant | LOW | c.1463+5G>A| |
S156 |
5 | BAA01g08430 | A01 | 3722998 | G | A | missense_variant | MODERATE | c.1778G>A|p.Gly593Asp |
S52 |
6 | BAA01g08430 | A01 | 3725633 | C | T | splice_region_variant&intron_variant | LOW | c.2932+7C>T| |
S36 |
7 | BAA01g08430 | A01 | 3726415 | G | A | downstream_gene_variant | MODIFIER | c.*542G>A| |
S234 |
8 | BAA01g08430 | A01 | 3729309 | G | A | downstream_gene_variant | MODIFIER | c.*3436G>A| |
S224 |