Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g44290 | A03 | 21018954 | G | A | downstream_gene_variant | MODIFIER | c.*2138C>T| |
S257 |
2 | BAA03g44290 | A03 | 21019228 | G | A | downstream_gene_variant | MODIFIER | c.*1864C>T| |
S236 |
3 | BAA03g44290 | A03 | 21021109 | C | T | missense_variant | MODERATE | c.1561G>A|p.Glu521Lys |
S158 |
4 | BAA03g44290 | A03 | 21021159 | G | A | missense_variant | MODERATE | c.1511C>T|p.Ala504Val |
S226 |
5 | BAA03g44290 | A03 | 21021598 | G | A | stop_gained | HIGH | c.1072C>T|p.Gln358* |
S25 |
6 | BAA03g44290 | A03 | 21022610 | A | T | missense_variant | MODERATE | c.487T>A|p.Ser163Thr |
S14 |
7 | BAA03g44290 | A03 | 21023049 | G | A | synonymous_variant | LOW | c.48C>T|p.Leu16Leu |
S56 |
8 | BAA03g44290 | A03 | 21024147 | G | A | upstream_gene_variant | MODIFIER | c.-1051C>T| |
S180 |
9 | BAA03g44290 | A03 | 21024375 | C | T | upstream_gene_variant | MODIFIER | c.-1279G>A| |
S165 |
10 | BAA03g44290 | A03 | 21024398 | G | T | upstream_gene_variant | MODIFIER | c.-1302C>A| |
S171 |
11 | BAA03g44290 | A03 | 21024401 | C | T | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S266 |
12 | BAA03g44290 | A03 | 21024702 | C | T | upstream_gene_variant | MODIFIER | c.-1606G>A| |
S161 |
13 | BAA03g44290 | A03 | 21024807 | C | T | upstream_gene_variant | MODIFIER | c.-1711G>A| |
S159 |
14 | BAA03g44290 | A03 | 21025672 | G | A | upstream_gene_variant | MODIFIER | c.-2576C>T| |
S269 |
15 | BAA03g44290 | A03 | 21027725 | C | T | upstream_gene_variant | MODIFIER | c.-4629G>A| |
S281 |