Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00260 | A02 | 152668 | C | T | missense_variant | MODERATE | c.1207G>A|p.Asp403Asn |
S40 S49 |
2 | BAA02g00260 | A02 | 152791 | C | T | missense_variant | MODERATE | c.1084G>A|p.Glu362Lys |
S167 |
3 | BAA02g00260 | A02 | 152928 | C | T | missense_variant&splice_region_variant | MODERATE | c.947G>A|p.Gly316Glu |
S47 |
4 | BAA02g00260 | A02 | 155543 | C | T | upstream_gene_variant | MODIFIER | c.-1163G>A| |
S172 S217 |
5 | BAA02g00260 | A02 | 155550 | G | A | upstream_gene_variant | MODIFIER | c.-1170C>T| |
S165 |
6 | BAA02g00260 | A02 | 155560 | C | T | upstream_gene_variant | MODIFIER | c.-1180G>A| |
S181 |
7 | BAA02g00260 | A02 | 156529 | C | T | upstream_gene_variant | MODIFIER | c.-2149G>A| |
S180 |
8 | BAA02g00260 | A02 | 157141 | C | T | upstream_gene_variant | MODIFIER | c.-2761G>A| |
S274 |
9 | BAA02g00260 | A02 | 157625 | C | T | upstream_gene_variant | MODIFIER | c.-3245G>A| |
S19 |