Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42620 | A02 | 35461376 | C | T | upstream_gene_variant | MODIFIER | c.-4622C>T| |
S3 |
2 | BAA02g42620 | A02 | 35461575 | C | T | upstream_gene_variant | MODIFIER | c.-4423C>T| |
S118 S58 |
3 | BAA02g42620 | A02 | 35461757 | C | T | upstream_gene_variant | MODIFIER | c.-4241C>T| |
S97 |
4 | BAA02g42620 | A02 | 35461991 | G | A | upstream_gene_variant | MODIFIER | c.-4007G>A| |
S7 |
5 | BAA02g42620 | A02 | 35462697 | C | T | upstream_gene_variant | MODIFIER | c.-3301C>T| |
S107 |
6 | BAA02g42620 | A02 | 35464074 | G | A | upstream_gene_variant | MODIFIER | c.-1924G>A| |
S41 |
7 | BAA02g42620 | A02 | 35465706 | G | A | upstream_gene_variant | MODIFIER | c.-292G>A| |
S247 |
8 | BAA02g42620 | A02 | 35466121 | C | T | missense_variant | MODERATE | c.124C>T|p.Leu42Phe |
S267 |
9 | BAA02g42620 | A02 | 35468015 | C | T | synonymous_variant | LOW | c.963C>T|p.Phe321Phe |
S39 |
10 | BAA02g42620 | A02 | 35468083 | C | T | missense_variant | MODERATE | c.1031C>T|p.Ser344Leu |
S109 |
11 | BAA02g42620 | A02 | 35468685 | G | A | splice_region_variant&intron_variant | LOW | c.1305+5G>A| |
S143 |