Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11630 | A01 | 5375023 | C | T | missense_variant | MODERATE | c.304C>T|p.Pro102Ser |
S47 |
2 | BAA01g11630 | A01 | 5375664 | C | T | missense_variant | MODERATE | c.784C>T|p.Leu262Phe |
S50 |
3 | BAA01g11630 | A01 | 5376429 | C | T | missense_variant | MODERATE | c.1315C>T|p.Arg439Trp |
S144 |
4 | BAA01g11630 | A01 | 5377869 | C | T | downstream_gene_variant | MODIFIER | c.*783C>T| |
S305 |
5 | BAA01g11630 | A01 | 5377889 | G | A | downstream_gene_variant | MODIFIER | c.*803G>A| |
S3 |
6 | BAA01g11630 | A01 | 5378131 | C | T | downstream_gene_variant | MODIFIER | c.*1045C>T| |
S100 |
7 | BAA01g11630 | A01 | 5379427 | G | A | downstream_gene_variant | MODIFIER | c.*2341G>A| |
S195 |
8 | BAA01g11630 | A01 | 5379637 | C | T | downstream_gene_variant | MODIFIER | c.*2551C>T| |
S202 |
9 | BAA01g11630 | A01 | 5379651 | C | T | downstream_gene_variant | MODIFIER | c.*2565C>T| |
S295 |
10 | BAA01g11630 | A01 | 5379673 | C | T | downstream_gene_variant | MODIFIER | c.*2587C>T| |
S118 |
11 | BAA01g11630 | A01 | 5379919 | C | T | downstream_gene_variant | MODIFIER | c.*2833C>T| |
S278 |