Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14530 | A10 | 15188424 | C | T | synonymous_variant | LOW | c.786C>T|p.Phe262Phe |
S121 |
2 | BAA10g14530 | A10 | 15188798 | C | T | missense_variant | MODERATE | c.1160C>T|p.Ser387Phe |
S229 |
3 | BAA10g14530 | A10 | 15189474 | G | A | missense_variant&splice_region_variant | MODERATE | c.1654G>A|p.Gly552Arg |
S192 |
4 | BAA10g14530 | A10 | 15189479 | C | T | splice_region_variant&intron_variant | LOW | c.1655+4C>T| |
S225 S73 |
5 | BAA10g14530 | A10 | 15191840 | G | A | downstream_gene_variant | MODIFIER | c.*1784G>A| |
S167 |
6 | BAA10g14530 | A10 | 15191996 | C | T | downstream_gene_variant | MODIFIER | c.*1940C>T| |
S206 |
7 | BAA10g14530 | A10 | 15193004 | C | T | downstream_gene_variant | MODIFIER | c.*2948C>T| |
S176 |