Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00660 | A09 | 584193 | C | T | stop_gained | HIGH | c.22C>T|p.Gln8* |
S133 |
2 | BAA09g00660 | A09 | 584363 | C | T | synonymous_variant | LOW | c.111C>T|p.Leu37Leu |
S171 |
3 | BAA09g00660 | A09 | 584943 | C | T | missense_variant | MODERATE | c.458C>T|p.Ser153Phe |
S261 S274 S303 |
4 | BAA09g00660 | A09 | 585949 | C | T | missense_variant&splice_region_variant | MODERATE | c.959C>T|p.Thr320Ile |
S171 |
5 | BAA09g00660 | A09 | 586854 | G | A | missense_variant | MODERATE | c.1345G>A|p.Val449Ile |
S206 |
6 | BAA09g00660 | A09 | 587651 | G | A | synonymous_variant | LOW | c.2142G>A|p.Arg714Arg |
S46 |
7 | BAA09g00660 | A09 | 588025 | C | T | missense_variant | MODERATE | c.2516C>T|p.Pro839Leu |
S288 |
8 | BAA09g00660 | A09 | 589230 | G | A | downstream_gene_variant | MODIFIER | c.*734G>A| |
S281 |
9 | BAA09g00660 | A09 | 591055 | G | A | downstream_gene_variant | MODIFIER | c.*2559G>A| |
S6 |
10 | BAA09g00660 | A09 | 592779 | C | T | downstream_gene_variant | MODIFIER | c.*4283C>T| |
S158 |