Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46600 | A02 | 37844882 | G | A | missense_variant | MODERATE | c.1219C>T|p.Pro407Ser |
S152 |
2 | BAA02g46600 | A02 | 37844885 | G | A | missense_variant | MODERATE | c.1216C>T|p.Pro406Ser |
S251 |
3 | BAA02g46600 | A02 | 37845496 | C | A | missense_variant | MODERATE | c.605G>T|p.Arg202Ile |
S202 |
4 | BAA02g46600 | A02 | 37846408 | G | A | upstream_gene_variant | MODIFIER | c.-104C>T| |
S36 |
5 | BAA02g46600 | A02 | 37847257 | C | T | upstream_gene_variant | MODIFIER | c.-953G>A| |
S53 |
6 | BAA02g46600 | A02 | 37847478 | C | T | upstream_gene_variant | MODIFIER | c.-1174G>A| |
S189 |
7 | BAA02g46600 | A02 | 37847486 | G | A | upstream_gene_variant | MODIFIER | c.-1182C>T| |
S264 |
8 | BAA02g46600 | A02 | 37848989 | G | A | upstream_gene_variant | MODIFIER | c.-2685C>T| |
S274 |
9 | BAA02g46600 | A02 | 37850597 | G | A | upstream_gene_variant | MODIFIER | c.-4293C>T| |
S25 |