Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g34260 | A08 | 22120353 | G | A | missense_variant | MODERATE | c.2240C>T|p.Thr747Ile |
S218 |
2 | BAA08g34260 | A08 | 22120416 | G | A | missense_variant | MODERATE | c.2177C>T|p.Ser726Phe |
S78 S83 |
3 | BAA08g34260 | A08 | 22120472 | G | A | synonymous_variant | LOW | c.2121C>T|p.Leu707Leu |
S242 |
4 | BAA08g34260 | A08 | 22121334 | C | T | missense_variant | MODERATE | c.1540G>A|p.Asp514Asn |
S159 S243 |
5 | BAA08g34260 | A08 | 22122761 | C | T | splice_region_variant&intron_variant | LOW | c.923-4G>A| |
S6 |
6 | BAA08g34260 | A08 | 22123510 | C | T | missense_variant | MODERATE | c.594G>A|p.Met198Ile |
S201 |
7 | BAA08g34260 | A08 | 22125529 | G | A | upstream_gene_variant | MODIFIER | c.-583C>T| |
S236 |
8 | BAA08g34260 | A08 | 22127008 | G | A | upstream_gene_variant | MODIFIER | c.-2062C>T| |
S190 |
9 | BAA08g34260 | A08 | 22127826 | G | A | upstream_gene_variant | MODIFIER | c.-2880C>T| |
S139 |