Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46930 | A02 | 38003890 | C | T | missense_variant | MODERATE | c.1040G>A|p.Gly347Glu |
S129 |
2 | BAA02g46930 | A02 | 38004016 | C | T | missense_variant | MODERATE | c.914G>A|p.Ser305Asn |
S303 |
3 | BAA02g46930 | A02 | 38004378 | G | A | synonymous_variant | LOW | c.552C>T|p.Ile184Ile |
S280 |
4 | BAA02g46930 | A02 | 38004488 | C | T | missense_variant | MODERATE | c.442G>A|p.Ala148Thr |
S77 S82 |
5 | BAA02g46930 | A02 | 38004776 | G | A | missense_variant | MODERATE | c.154C>T|p.Pro52Ser |
S231 |
6 | BAA02g46930 | A02 | 38005250 | C | T | upstream_gene_variant | MODIFIER | c.-321G>A| |
S1 S90 |
7 | BAA02g46930 | A02 | 38005917 | G | A | upstream_gene_variant | MODIFIER | c.-988C>T| |
S143 |
8 | BAA02g46930 | A02 | 38006406 | G | A | upstream_gene_variant | MODIFIER | c.-1477C>T| |
S200 |
9 | BAA02g46930 | A02 | 38007481 | C | T | upstream_gene_variant | MODIFIER | c.-2552G>A| |
S233 |
10 | BAA02g46930 | A02 | 38008135 | G | A | upstream_gene_variant | MODIFIER | c.-3206C>T| |
S308 |
11 | BAA02g46930 | A02 | 38008367 | C | T | upstream_gene_variant | MODIFIER | c.-3438G>A| |
S262 |