Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g26200 | A03 | 12021880 | G | A | missense_variant | MODERATE | c.1598C>T|p.Ala533Val |
S65 |
2 | BAA03g26200 | A03 | 12022007 | C | T | missense_variant | MODERATE | c.1471G>A|p.Ala491Thr |
S293 |
3 | BAA03g26200 | A03 | 12022659 | G | A | missense_variant | MODERATE | c.980C>T|p.Ala327Val |
S234 |
4 | BAA03g26200 | A03 | 12022718 | G | A | synonymous_variant | LOW | c.921C>T|p.Leu307Leu |
S294 |
5 | BAA03g26200 | A03 | 12022840 | T | C | missense_variant | MODERATE | c.799A>G|p.Ile267Val |
S211 S227 |
6 | BAA03g26200 | A03 | 12022919 | G | A | synonymous_variant | LOW | c.720C>T|p.Ile240Ile |
S288 |
7 | BAA03g26200 | A03 | 12024509 | G | A | upstream_gene_variant | MODIFIER | c.-441C>T| |
S70 |
8 | BAA03g26200 | A03 | 12024533 | C | T | upstream_gene_variant | MODIFIER | c.-465G>A| |
S164 |
9 | BAA03g26200 | A03 | 12024625 | C | T | upstream_gene_variant | MODIFIER | c.-557G>A| |
S164 |
10 | BAA03g26200 | A03 | 12024732 | C | T | upstream_gene_variant | MODIFIER | c.-664G>A| |
S132 S215 |
11 | BAA03g26200 | A03 | 12024872 | G | A | upstream_gene_variant | MODIFIER | c.-804C>T| |
S257 |
12 | BAA03g26200 | A03 | 12027125 | G | A | upstream_gene_variant | MODIFIER | c.-3057C>T| |
S296 |
13 | BAA03g26200 | A03 | 12027246 | C | T | upstream_gene_variant | MODIFIER | c.-3178G>A| |
S19 |
14 | BAA03g26200 | A03 | 12027531 | G | A | upstream_gene_variant | MODIFIER | c.-3463C>T| |
S247 |
15 | BAA03g26200 | A03 | 12028082 | G | A | upstream_gene_variant | MODIFIER | c.-4014C>T| |
S138 |