Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g23440 | A08 | 17322134 | C | T | upstream_gene_variant | MODIFIER | c.-373C>T| |
S64 |
2 | BAA08g23440 | A08 | 17322588 | G | A | intron_variant | MODIFIER | c.36+46G>A| |
S48 |
3 | BAA08g23440 | A08 | 17322902 | C | T | intron_variant | MODIFIER | c.189+32C>T| |
S223 |
4 | BAA08g23440 | A08 | 17323078 | C | T | intron_variant | MODIFIER | c.297+24C>T| |
S171 |
5 | BAA08g23440 | A08 | 17323087 | C | T | intron_variant | MODIFIER | c.297+33C>T| |
S303 |
6 | BAA08g23440 | A08 | 17323422 | G | A | missense_variant | MODERATE | c.496G>A|p.Glu166Lys |
S65 |
7 | BAA08g23440 | A08 | 17323628 | G | A | missense_variant | MODERATE | c.622G>A|p.Ala208Thr |
S218 |
8 | BAA08g23440 | A08 | 17323737 | C | T | missense_variant | MODERATE | c.731C>T|p.Pro244Leu |
S67 |
9 | BAA08g23440 | A08 | 17326646 | G | A | synonymous_variant | LOW | c.2133G>A|p.Arg711Arg |
S193 |
10 | BAA08g23440 | A08 | 17326763 | G | A | missense_variant | MODERATE | c.2250G>A|p.Met750Ile |
S298 |
11 | BAA08g23440 | A08 | 17327247 | C | T | synonymous_variant | LOW | c.2454C>T|p.Pro818Pro |
S121 |