Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41950 | A02 | 35025083 | C | T | synonymous_variant | LOW | c.3084G>A|p.Gly1028Gly |
S296 |
2 | BAA02g41950 | A02 | 35026079 | G | A | missense_variant | MODERATE | c.2648C>T|p.Ser883Phe |
S57 |
3 | BAA02g41950 | A02 | 35027096 | G | A | missense_variant | MODERATE | c.2362C>T|p.Leu788Phe |
S79 S91 |
4 | BAA02g41950 | A02 | 35027235 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2224-1G>A| |
S1 |
5 | BAA02g41950 | A02 | 35028528 | G | A | missense_variant | MODERATE | c.1585C>T|p.Pro529Ser |
S144 |
6 | BAA02g41950 | A02 | 35030099 | C | T | missense_variant | MODERATE | c.716G>A|p.Gly239Glu |
S165 |
7 | BAA02g41950 | A02 | 35030287 | G | A | missense_variant | MODERATE | c.677C>T|p.Ala226Val |
S251 |
8 | BAA02g41950 | A02 | 35030359 | G | A | missense_variant | MODERATE | c.605C>T|p.Ser202Phe |
S4 |
9 | BAA02g41950 | A02 | 35032062 | C | T | upstream_gene_variant | MODIFIER | c.-32G>A| |
S172 S217 |
10 | BAA02g41950 | A02 | 35032099 | G | A | upstream_gene_variant | MODIFIER | c.-69C>T| |
S188 |
11 | BAA02g41950 | A02 | 35032519 | C | T | upstream_gene_variant | MODIFIER | c.-489G>A| |
S46 |
12 | BAA02g41950 | A02 | 35034033 | G | A | upstream_gene_variant | MODIFIER | c.-2003C>T| |
S127 |