Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16940 | A02 | 8395501 | G | A | missense_variant | MODERATE | c.2746C>T|p.Pro916Ser |
S94 |
2 | BAA02g16940 | A02 | 8396376 | C | T | missense_variant | MODERATE | c.2026G>A|p.Asp676Asn |
S267 |
3 | BAA02g16940 | A02 | 8396635 | C | T | missense_variant | MODERATE | c.1921G>A|p.Asp641Asn |
S302 |
4 | BAA02g16940 | A02 | 8397135 | G | A | synonymous_variant | LOW | c.1512C>T|p.Phe504Phe |
S105 S106 |
5 | BAA02g16940 | A02 | 8397245 | C | T | missense_variant | MODERATE | c.1402G>A|p.Glu468Lys |
S116 |
6 | BAA02g16940 | A02 | 8398019 | G | A | synonymous_variant | LOW | c.798C>T|p.Ser266Ser |
S37 |
7 | BAA02g16940 | A02 | 8398102 | G | A | missense_variant | MODERATE | c.715C>T|p.Leu239Phe |
S2 |
8 | BAA02g16940 | A02 | 8398511 | C | T | intron_variant | MODIFIER | c.579-273G>A| |
S238 |
9 | BAA02g16940 | A02 | 8398514 | G | A | intron_variant | MODIFIER | c.579-276C>T| |
S257 |
10 | BAA02g16940 | A02 | 8399616 | C | T | upstream_gene_variant | MODIFIER | c.-41G>A| |
S220 S5 |
11 | BAA02g16940 | A02 | 8399952 | C | T | upstream_gene_variant | MODIFIER | c.-377G>A| |
S138 |
12 | BAA02g16940 | A02 | 8401028 | C | T | upstream_gene_variant | MODIFIER | c.-1453G>A| |
S224 |
13 | BAA02g16940 | A02 | 8401071 | G | A | upstream_gene_variant | MODIFIER | c.-1496C>T| |
S247 |
14 | BAA02g16940 | A02 | 8402255 | G | A | upstream_gene_variant | MODIFIER | c.-2680C>T| |
S74 |
15 | BAA02g16940 | A02 | 8404218 | G | A | upstream_gene_variant | MODIFIER | c.-4643C>T| |
S4 |