Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g09390 | A09 | 5211639 | G | A | upstream_gene_variant | MODIFIER | c.-1526G>A| |
S200 |
2 | BAA09g09390 | A09 | 5213429 | G | A | missense_variant | MODERATE | c.265G>A|p.Gly89Arg |
S16 |
3 | BAA09g09390 | A09 | 5213536 | G | A | synonymous_variant | LOW | c.372G>A|p.Leu124Leu |
S240 |
4 | BAA09g09390 | A09 | 5213862 | C | T | missense_variant | MODERATE | c.698C>T|p.Pro233Leu |
S94 |
5 | BAA09g09390 | A09 | 5213911 | G | A | synonymous_variant | LOW | c.747G>A|p.Gln249Gln |
S189 |
6 | BAA09g09390 | A09 | 5213915 | G | A | missense_variant | MODERATE | c.751G>A|p.Gly251Ser |
S126 |
7 | BAA09g09390 | A09 | 5214230 | G | A | missense_variant | MODERATE | c.1066G>A|p.Gly356Ser |
S167 |
8 | BAA09g09390 | A09 | 5214410 | G | A | missense_variant | MODERATE | c.1246G>A|p.Asp416Asn |
S40 S49 |
9 | BAA09g09390 | A09 | 5214524 | C | T | missense_variant | MODERATE | c.1360C>T|p.Arg454Cys |
S173 |
10 | BAA09g09390 | A09 | 5214686 | G | A | missense_variant | MODERATE | c.1522G>A|p.Glu508Lys |
S260 |
11 | BAA09g09390 | A09 | 5215751 | C | T | missense_variant | MODERATE | c.2587C>T|p.Pro863Ser |
S156 |