Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g22530 | A04 | 24905406 | A | C | missense_variant | MODERATE | c.40T>G|p.Phe14Val |
S147 S267 S91 |
2 | BAA04g22530 | A04 | 24905407 | T | A | synonymous_variant | LOW | c.39A>T|p.Ala13Ala |
S147 S267 S91 |
3 | BAA04g22530 | A04 | 24905427 | A | C | missense_variant | MODERATE | c.19T>G|p.Phe7Val |
S147 S201 S267 S91 |
4 | BAA04g22530 | A04 | 24905433 | T | C | missense_variant | MODERATE | c.13A>G|p.Thr5Ala |
S147 S201 S267 S91 |
5 | BAA04g22530 | A04 | 24908328 | G | A | upstream_gene_variant | MODIFIER | c.-2883C>T| |
S218 |
6 | BAA04g22530 | A04 | 24909631 | C | T | upstream_gene_variant | MODIFIER | c.-4186G>A| |
S292 |
7 | BAA04g22530 | A04 | 24909894 | C | T | upstream_gene_variant | MODIFIER | c.-4449G>A| |
S95 |
8 | BAA04g22530 | A04 | 24909944 | C | T | upstream_gene_variant | MODIFIER | c.-4499G>A| |
S172 S217 |
9 | BAA04g22530 | A04 | 24910382 | G | A | upstream_gene_variant | MODIFIER | c.-4937C>T| |
S281 |