Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21360 | A01 | 10595858 | C | T | synonymous_variant | LOW | c.504C>T|p.Tyr168Tyr |
S53 |
2 | BAA01g21360 | A01 | 10595961 | C | T | missense_variant | MODERATE | c.538C>T|p.Pro180Ser |
S289 S290 |
3 | BAA01g21360 | A01 | 10596190 | C | T | missense_variant | MODERATE | c.679C>T|p.Pro227Ser |
S46 |
4 | BAA01g21360 | A01 | 10597343 | G | A | missense_variant | MODERATE | c.1274G>A|p.Gly425Glu |
S181 |
5 | BAA01g21360 | A01 | 10598679 | G | A | missense_variant | MODERATE | c.1945G>A|p.Glu649Lys |
S240 |
6 | BAA01g21360 | A01 | 10598712 | G | A | missense_variant | MODERATE | c.1978G>A|p.Gly660Arg |
S262 |
7 | BAA01g21360 | A01 | 10598832 | G | A | missense_variant | MODERATE | c.2029G>A|p.Gly677Arg |
S71 |
8 | BAA01g21360 | A01 | 10598987 | G | A | synonymous_variant | LOW | c.2184G>A|p.Glu728Glu |
S116 |
9 | BAA01g21360 | A01 | 10601381 | C | T | synonymous_variant | LOW | c.2794C>T|p.Leu932Leu |
S205 |
10 | BAA01g21360 | A01 | 10601419 | C | T | synonymous_variant | LOW | c.2832C>T|p.Ser944Ser |
S179 |
11 | BAA01g21360 | A01 | 10603095 | C | T | downstream_gene_variant | MODIFIER | c.*1658C>T| |
S19 |
12 | BAA01g21360 | A01 | 10603516 | G | T | downstream_gene_variant | MODIFIER | c.*2079G>T| |
S98 |
13 | BAA01g21360 | A01 | 10603537 | C | T | downstream_gene_variant | MODIFIER | c.*2100C>T| |
S179 |