Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04590 | A02 | 1987715 | C | T | missense_variant | MODERATE | c.1546G>A|p.Glu516Lys |
S38 |
2 | BAA02g04590 | A02 | 1987847 | G | A | missense_variant | MODERATE | c.1414C>T|p.Leu472Phe |
S148 S210 S30 S31 |
3 | BAA02g04590 | A02 | 1987912 | C | T | missense_variant | MODERATE | c.1349G>A|p.Gly450Glu |
S186 |
4 | BAA02g04590 | A02 | 1989270 | G | A | synonymous_variant | LOW | c.303C>T|p.Tyr101Tyr |
S295 |
5 | BAA02g04590 | A02 | 1989609 | C | T | missense_variant | MODERATE | c.124G>A|p.Asp42Asn |
S245 |
6 | BAA02g04590 | A02 | 1989661 | C | T | synonymous_variant | LOW | c.72G>A|p.Lys24Lys |
S95 |
7 | BAA02g04590 | A02 | 1992998 | C | T | upstream_gene_variant | MODIFIER | c.-3266G>A| |
S152 |
8 | BAA02g04590 | A02 | 1993021 | C | T | upstream_gene_variant | MODIFIER | c.-3289G>A| |
S58 |
9 | BAA02g04590 | A02 | 1993525 | C | T | upstream_gene_variant | MODIFIER | c.-3793G>A| |
S75 |