Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14450 | A08 | 12329126 | C | T | missense_variant | MODERATE | c.752C>T|p.Ser251Phe |
S243 |
2 | BAA08g14450 | A08 | 12329697 | G | A | intron_variant | MODIFIER | c.849+474G>A| |
S35 |
3 | BAA08g14450 | A08 | 12330102 | G | A | intron_variant | MODIFIER | c.849+879G>A| |
S280 |
4 | BAA08g14450 | A08 | 12330604 | C | T | intron_variant | MODIFIER | c.850-538C>T| |
S79 S84 |
5 | BAA08g14450 | A08 | 12332041 | C | T | intron_variant | MODIFIER | c.965-383C>T| |
S162 |
6 | BAA08g14450 | A08 | 12332379 | G | A | intron_variant | MODIFIER | c.965-45G>A| |
S46 |
7 | BAA08g14450 | A08 | 12332848 | G | A | downstream_gene_variant | MODIFIER | c.*165G>A| |
S30 |
8 | BAA08g14450 | A08 | 12333405 | G | A | downstream_gene_variant | MODIFIER | c.*722G>A| |
S81 S85 |
9 | BAA08g14450 | A08 | 12333778 | C | T | downstream_gene_variant | MODIFIER | c.*1095C>T| |
S43 |