Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20950 | A09 | 12981943 | C | T | missense_variant | MODERATE | c.1132G>A|p.Gly378Ser |
S11 |
2 | BAA09g20950 | A09 | 12982347 | G | A | missense_variant | MODERATE | c.728C>T|p.Thr243Ile |
S205 |
3 | BAA09g20950 | A09 | 12982462 | G | A | missense_variant | MODERATE | c.613C>T|p.Leu205Phe |
S196 |
4 | BAA09g20950 | A09 | 12982662 | C | T | missense_variant | MODERATE | c.413G>A|p.Gly138Glu |
S15 S3 |
5 | BAA09g20950 | A09 | 12983032 | C | T | missense_variant | MODERATE | c.188G>A|p.Gly63Asp |
S182 |
6 | BAA09g20950 | A09 | 12984164 | G | A | upstream_gene_variant | MODIFIER | c.-945C>T| |
S238 |
7 | BAA09g20950 | A09 | 12984254 | C | T | upstream_gene_variant | MODIFIER | c.-1035G>A| |
S272 |
8 | BAA09g20950 | A09 | 12984775 | G | A | upstream_gene_variant | MODIFIER | c.-1556C>T| |
S32 S4 |
9 | BAA09g20950 | A09 | 12985507 | C | T | upstream_gene_variant | MODIFIER | c.-2288G>A| |
S255 |
10 | BAA09g20950 | A09 | 12985616 | C | T | upstream_gene_variant | MODIFIER | c.-2397G>A| |
S150 |
11 | BAA09g20950 | A09 | 12985716 | C | T | upstream_gene_variant | MODIFIER | c.-2497G>A| |
S187 |
12 | BAA09g20950 | A09 | 12987025 | C | T | upstream_gene_variant | MODIFIER | c.-3806G>A| |
S206 S26 |