Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66430 | A03 | 40751005 | C | T | downstream_gene_variant | MODIFIER | c.*652G>A| |
S75 |
2 | BAA03g66430 | A03 | 40751748 | C | T | missense_variant | MODERATE | c.1766G>A|p.Gly589Glu |
S207 |
3 | BAA03g66430 | A03 | 40751934 | C | T | missense_variant | MODERATE | c.1580G>A|p.Gly527Glu |
S120 |
4 | BAA03g66430 | A03 | 40752090 | G | A | missense_variant | MODERATE | c.1424C>T|p.Ala475Val |
S183 S198 |
5 | BAA03g66430 | A03 | 40752184 | G | A | missense_variant | MODERATE | c.1330C>T|p.Pro444Ser |
S241 |
6 | BAA03g66430 | A03 | 40752698 | C | T | missense_variant | MODERATE | c.902G>A|p.Arg301Gln |
S76 |
7 | BAA03g66430 | A03 | 40753440 | C | T | synonymous_variant | LOW | c.237G>A|p.Lys79Lys |
S188 |
8 | BAA03g66430 | A03 | 40753501 | T | G | missense_variant | MODERATE | c.176A>C|p.Asn59Thr |
S165 S211 S227 |
9 | BAA03g66430 | A03 | 40753660 | C | T | missense_variant | MODERATE | c.17G>A|p.Gly6Asp |
S159 |
10 | BAA03g66430 | A03 | 40753693 | G | A | upstream_gene_variant | MODIFIER | c.-17C>T| |
S181 |
11 | BAA03g66430 | A03 | 40754058 | C | T | upstream_gene_variant | MODIFIER | c.-382G>A| |
S95 |
12 | BAA03g66430 | A03 | 40754779 | C | T | upstream_gene_variant | MODIFIER | c.-1103G>A| |
S105 S106 |
13 | BAA03g66430 | A03 | 40754846 | C | T | upstream_gene_variant | MODIFIER | c.-1170G>A| |
S20 |
14 | BAA03g66430 | A03 | 40754872 | C | T | upstream_gene_variant | MODIFIER | c.-1196G>A| |
S108 |
15 | BAA03g66430 | A03 | 40755121 | G | A | upstream_gene_variant | MODIFIER | c.-1445C>T| |
S82 S92 |
16 | BAA03g66430 | A03 | 40756274 | G | A | upstream_gene_variant | MODIFIER | c.-2598C>T| |
S7 |
17 | BAA03g66430 | A03 | 40756671 | G | A | upstream_gene_variant | MODIFIER | c.-2995C>T| |
S236 |
18 | BAA03g66430 | A03 | 40757133 | G | A | upstream_gene_variant | MODIFIER | c.-3457C>T| |
S171 |
19 | BAA03g66430 | A03 | 40757910 | G | A | upstream_gene_variant | MODIFIER | c.-4234C>T| |
S224 |