Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18180 | A01 | 8931817 | C | T | missense_variant | MODERATE | c.1756G>A|p.Val586Met |
S179 |
2 | BAA01g18180 | A01 | 8932349 | G | A | missense_variant | MODERATE | c.1693C>T|p.Leu565Phe |
S183 |
3 | BAA01g18180 | A01 | 8937053 | G | A | intron_variant | MODIFIER | c.1469+324C>T| |
S139 |
4 | BAA01g18180 | A01 | 8937230 | G | A | intron_variant | MODIFIER | c.1469+147C>T| |
S131 |
5 | BAA01g18180 | A01 | 8939091 | G | A | intron_variant | MODIFIER | c.391-26C>T| |
S27 |
6 | BAA01g18180 | A01 | 8939280 | G | A | splice_region_variant&intron_variant | LOW | c.253-5C>T| |
S105 S106 |
7 | BAA01g18180 | A01 | 8940737 | G | A | upstream_gene_variant | MODIFIER | c.-597C>T| |
S212 |
8 | BAA01g18180 | A01 | 8940912 | G | A | upstream_gene_variant | MODIFIER | c.-772C>T| |
S181 |
9 | BAA01g18180 | A01 | 8943842 | T | G | upstream_gene_variant | MODIFIER | c.-3702A>C| |
S169 S251 S289 |
10 | BAA01g18180 | A01 | 8944374 | C | T | upstream_gene_variant | MODIFIER | c.-4234G>A| |
S42 |