Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g25780 | A04 | 26681093 | C | T | missense_variant | MODERATE | c.79C>T|p.Leu27Phe |
S180 |
2 | BAA04g25780 | A04 | 26681447 | C | T | missense_variant | MODERATE | c.433C>T|p.Leu145Phe |
S149 |
3 | BAA04g25780 | A04 | 26681727 | G | A | missense_variant | MODERATE | c.713G>A|p.Arg238Lys |
S251 |
4 | BAA04g25780 | A04 | 26682306 | C | T | missense_variant | MODERATE | c.1214C>T|p.Ala405Val |
S294 |
5 | BAA04g25780 | A04 | 26682908 | G | A | missense_variant | MODERATE | c.1637G>A|p.Arg546Gln |
S231 |
6 | BAA04g25780 | A04 | 26683537 | G | A | missense_variant | MODERATE | c.1790G>A|p.Ser597Asn |
S71 |
7 | BAA04g25780 | A04 | 26683677 | G | A | missense_variant | MODERATE | c.1930G>A|p.Gly644Ser |
S52 |
8 | BAA04g25780 | A04 | 26684052 | C | T | synonymous_variant | LOW | c.2223C>T|p.Phe741Phe |
S139 |
9 | BAA04g25780 | A04 | 26685608 | G | A | downstream_gene_variant | MODIFIER | c.*1448G>A| |
S126 |
10 | BAA04g25780 | A04 | 26685929 | C | T | downstream_gene_variant | MODIFIER | c.*1769C>T| |
S174 S216 S241 |
11 | BAA04g25780 | A04 | 26685954 | C | T | downstream_gene_variant | MODIFIER | c.*1794C>T| |
S48 |
12 | BAA04g25780 | A04 | 26687690 | C | T | downstream_gene_variant | MODIFIER | c.*3530C>T| |
S107 |