Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02290 | A01 | 1053980 | G | A | synonymous_variant | LOW | c.1305C>T|p.Ala435Ala |
S284 |
2 | BAA01g02290 | A01 | 1054014 | C | T | missense_variant | MODERATE | c.1271G>A|p.Gly424Glu |
S140 |
3 | BAA01g02290 | A01 | 1054302 | G | A | missense_variant | MODERATE | c.983C>T|p.Pro328Leu |
S9 |
4 | BAA01g02290 | A01 | 1054391 | G | A | synonymous_variant | LOW | c.894C>T|p.Ile298Ile |
S33 |
5 | BAA01g02290 | A01 | 1054491 | C | T | missense_variant | MODERATE | c.794G>A|p.Arg265Gln |
S133 S203 |
6 | BAA01g02290 | A01 | 1054501 | C | T | missense_variant | MODERATE | c.784G>A|p.Gly262Arg |
S171 |
7 | BAA01g02290 | A01 | 1059068 | G | A | upstream_gene_variant | MODIFIER | c.-3784C>T| |
S263 |
8 | BAA01g02290 | A01 | 1059071 | G | A | upstream_gene_variant | MODIFIER | c.-3787C>T| |
S239 |
9 | BAA01g02290 | A01 | 1059561 | G | A | upstream_gene_variant | MODIFIER | c.-4277C>T| |
S272 |
10 | BAA01g02290 | A01 | 1059868 | G | A | upstream_gene_variant | MODIFIER | c.-4584C>T| |
S293 |
11 | BAA01g02290 | A01 | 1060022 | C | T | upstream_gene_variant | MODIFIER | c.-4738G>A| |
S205 |