Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g38700 | A05 | 38004372 | C | T | missense_variant | MODERATE | c.137C>T|p.Ser46Phe |
S35 |
2 | BAA05g38700 | A05 | 38004466 | C | T | synonymous_variant | LOW | c.231C>T|p.Leu77Leu |
S255 |
3 | BAA05g38700 | A05 | 38004474 | G | A | missense_variant | MODERATE | c.239G>A|p.Gly80Asp |
S47 |
4 | BAA05g38700 | A05 | 38005965 | C | T | missense_variant | MODERATE | c.869C>T|p.Ser290Phe |
S281 |
5 | BAA05g38700 | A05 | 38006124 | G | A | missense_variant | MODERATE | c.1028G>A|p.Gly343Asp |
S75 S81 |
6 | BAA05g38700 | A05 | 38006433 | C | T | missense_variant | MODERATE | c.1337C>T|p.Thr446Ile |
S8 |
7 | BAA05g38700 | A05 | 38006652 | G | A | missense_variant | MODERATE | c.1556G>A|p.Arg519Lys |
S50 |
8 | BAA05g38700 | A05 | 38007227 | C | T | downstream_gene_variant | MODIFIER | c.*490C>T| |
S175 |
9 | BAA05g38700 | A05 | 38007349 | G | A | downstream_gene_variant | MODIFIER | c.*612G>A| |
S276 |
10 | BAA05g38700 | A05 | 38007439 | C | T | downstream_gene_variant | MODIFIER | c.*702C>T| |
S149 |