Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13660 | A08 | 11875850 | G | A | upstream_gene_variant | MODIFIER | c.-2161G>A| |
S149 S5 |
2 | BAA08g13660 | A08 | 11876319 | G | A | upstream_gene_variant | MODIFIER | c.-1692G>A| |
S61 |
3 | BAA08g13660 | A08 | 11878291 | G | A | missense_variant | MODERATE | c.281G>A|p.Arg94Lys |
S298 |
4 | BAA08g13660 | A08 | 11878507 | G | A | missense_variant | MODERATE | c.497G>A|p.Arg166Gln |
S217 S248 |
5 | BAA08g13660 | A08 | 11878508 | G | A | synonymous_variant | LOW | c.498G>A|p.Arg166Arg |
S8 |
6 | BAA08g13660 | A08 | 11878520 | C | T | splice_region_variant&intron_variant | LOW | c.504+6C>T| |
S58 |
7 | BAA08g13660 | A08 | 11879532 | G | A | missense_variant | MODERATE | c.1307G>A|p.Gly436Glu |
S32 |
8 | BAA08g13660 | A08 | 11880189 | G | A | missense_variant | MODERATE | c.1808G>A|p.Gly603Glu |
S68 |
9 | BAA08g13660 | A08 | 11880742 | G | A | stop_gained | HIGH | c.2361G>A|p.Trp787* |
S35 |
10 | BAA08g13660 | A08 | 11881651 | G | A | downstream_gene_variant | MODIFIER | c.*849G>A| |
S28 |
11 | BAA08g13660 | A08 | 11881939 | C | T | downstream_gene_variant | MODIFIER | c.*1137C>T| |
S169 |