Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g08730 | A04 | 6042450 | G | A | missense_variant | MODERATE | c.559C>T|p.Pro187Ser |
S13 |
2 | BAA04g08730 | A04 | 6042772 | G | A | synonymous_variant | LOW | c.237C>T|p.Tyr79Tyr |
S45 |
3 | BAA04g08730 | A04 | 6042791 | C | T | missense_variant | MODERATE | c.218G>A|p.Gly73Asp |
S148 S210 |
4 | BAA04g08730 | A04 | 6045633 | G | A | upstream_gene_variant | MODIFIER | c.-2625C>T| |
S28 |
5 | BAA04g08730 | A04 | 6046538 | G | A | upstream_gene_variant | MODIFIER | c.-3530C>T| |
S143 S154 S164 S201 S230 S306 S72 |
6 | BAA04g08730 | A04 | 6046560 | G | A | upstream_gene_variant | MODIFIER | c.-3552C>T| |
S181 |
7 | BAA04g08730 | A04 | 6046936 | G | A | upstream_gene_variant | MODIFIER | c.-3928C>T| |
S278 |
8 | BAA04g08730 | A04 | 6046989 | C | T | upstream_gene_variant | MODIFIER | c.-3981G>A| |
S25 |