Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g43300 | A05 | 40680356 | C | T | missense_variant | MODERATE | c.544G>A|p.Ala182Thr |
S157 S163 |
2 | BAA05g43300 | A05 | 40680750 | G | A | missense_variant | MODERATE | c.298C>T|p.Leu100Phe |
S189 |
3 | BAA05g43300 | A05 | 40680843 | C | T | missense_variant | MODERATE | c.205G>A|p.Asp69Asn |
S122 |
4 | BAA05g43300 | A05 | 40680965 | C | A | splice_region_variant&intron_variant | LOW | c.89-6G>T| |
S219 S278 S279 S64 S72 |
5 | BAA05g43300 | A05 | 40684026 | C | T | upstream_gene_variant | MODIFIER | c.-2913G>A| |
S177 |
6 | BAA05g43300 | A05 | 40684043 | G | A | upstream_gene_variant | MODIFIER | c.-2930C>T| |
S262 |
7 | BAA05g43300 | A05 | 40684052 | G | A | upstream_gene_variant | MODIFIER | c.-2939C>T| |
S247 |
8 | BAA05g43300 | A05 | 40684194 | G | A | upstream_gene_variant | MODIFIER | c.-3081C>T| |
S261 |
9 | BAA05g43300 | A05 | 40685045 | C | T | upstream_gene_variant | MODIFIER | c.-3932G>A| |
S111 |
10 | BAA05g43300 | A05 | 40685297 | G | A | upstream_gene_variant | MODIFIER | c.-4184C>T| |
S107 |
11 | BAA05g43300 | A05 | 40685677 | C | T | upstream_gene_variant | MODIFIER | c.-4564G>A| |
S52 |
12 | BAA05g43300 | A05 | 40685943 | G | A | upstream_gene_variant | MODIFIER | c.-4830C>T| |
S81 S85 |