Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02660 | A01 | 1217675 | C | T | missense_variant | MODERATE | c.1889G>A|p.Gly630Glu |
S99 |
2 | BAA01g02660 | A01 | 1217790 | G | A | synonymous_variant | LOW | c.1860C>T|p.Arg620Arg |
S12 |
3 | BAA01g02660 | A01 | 1218180 | G | A | synonymous_variant | LOW | c.1686C>T|p.Cys562Cys |
S153 |
4 | BAA01g02660 | A01 | 1220586 | T | A | missense_variant | MODERATE | c.395A>T|p.Gln132Leu |
S23 |
5 | BAA01g02660 | A01 | 1220986 | C | T | missense_variant | MODERATE | c.149G>A|p.Cys50Tyr |
S36 |
6 | BAA01g02660 | A01 | 1220990 | C | T | missense_variant | MODERATE | c.145G>A|p.Glu49Lys |
S302 |
7 | BAA01g02660 | A01 | 1222955 | A | G | upstream_gene_variant | MODIFIER | c.-1821T>C| |
S293 |
8 | BAA01g02660 | A01 | 1225055 | C | T | upstream_gene_variant | MODIFIER | c.-3921G>A| |
S128 |