Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g32700 | A04 | 30087897 | G | A | upstream_gene_variant | MODIFIER | c.-2336G>A| |
S153 S213 |
2 | BAA04g32700 | A04 | 30088318 | C | T | upstream_gene_variant | MODIFIER | c.-1915C>T| |
S208 S93 |
3 | BAA04g32700 | A04 | 30090413 | C | T | missense_variant | MODERATE | c.181C>T|p.Pro61Ser |
S132 S137 S215 S89 |
4 | BAA04g32700 | A04 | 30091192 | C | T | missense_variant | MODERATE | c.604C>T|p.Leu202Phe |
S189 |
5 | BAA04g32700 | A04 | 30091338 | C | T | synonymous_variant | LOW | c.654C>T|p.Val218Val |
S92 |
6 | BAA04g32700 | A04 | 30091797 | C | T | missense_variant | MODERATE | c.1036C>T|p.Leu346Phe |
S14 |
7 | BAA04g32700 | A04 | 30092112 | C | T | missense_variant | MODERATE | c.1270C>T|p.His424Tyr |
S289 S68 |
8 | BAA04g32700 | A04 | 30092270 | G | A | missense_variant | MODERATE | c.1351G>A|p.Val451Met |
S82 S92 |
9 | BAA04g32700 | A04 | 30092292 | C | T | missense_variant | MODERATE | c.1373C>T|p.Pro458Leu |
S30 S31 |
10 | BAA04g32700 | A04 | 30092499 | C | T | splice_region_variant&intron_variant | LOW | c.1475+4C>T| |
S296 |