Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19390 | A08 | 15265539 | G | A | synonymous_variant | LOW | c.183G>A|p.Glu61Glu |
S287 |
2 | BAA08g19390 | A08 | 15266846 | C | T | missense_variant | MODERATE | c.913C>T|p.His305Tyr |
S28 |
3 | BAA08g19390 | A08 | 15266901 | G | A | missense_variant | MODERATE | c.968G>A|p.Ser323Asn |
S94 |
4 | BAA08g19390 | A08 | 15267318 | G | A | missense_variant | MODERATE | c.1132G>A|p.Glu378Lys |
S151 S263 |
5 | BAA08g19390 | A08 | 15267466 | C | T | missense_variant | MODERATE | c.1280C>T|p.Thr427Ile |
S291 |
6 | BAA08g19390 | A08 | 15267646 | T | G | missense_variant | MODERATE | c.1460T>G|p.Ile487Ser |
S280 |
7 | BAA08g19390 | A08 | 15272038 | C | T | downstream_gene_variant | MODIFIER | c.*3653C>T| |
S57 |
8 | BAA08g19390 | A08 | 15272107 | G | A | downstream_gene_variant | MODIFIER | c.*3722G>A| |
S289 S290 |
9 | BAA08g19390 | A08 | 15272179 | C | T | downstream_gene_variant | MODIFIER | c.*3794C>T| |
S213 |