Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22060 | A01 | 10995425 | G | A | upstream_gene_variant | MODIFIER | c.-3907G>A| |
S251 |
2 | BAA01g22060 | A01 | 10997708 | C | T | upstream_gene_variant | MODIFIER | c.-1624C>T| |
S255 |
3 | BAA01g22060 | A01 | 10997864 | G | A | upstream_gene_variant | MODIFIER | c.-1468G>A| |
S155 |
4 | BAA01g22060 | A01 | 10997992 | G | A | upstream_gene_variant | MODIFIER | c.-1340G>A| |
S178 |
5 | BAA01g22060 | A01 | 10999820 | G | A | missense_variant | MODERATE | c.269G>A|p.Gly90Glu |
S294 |
6 | BAA01g22060 | A01 | 10999852 | C | T | missense_variant | MODERATE | c.301C>T|p.His101Tyr |
S277 |
7 | BAA01g22060 | A01 | 10999861 | G | A | missense_variant | MODERATE | c.310G>A|p.Glu104Lys |
S292 |
8 | BAA01g22060 | A01 | 11001065 | G | A | splice_donor_variant&intron_variant | HIGH | c.818+1G>A| |
S187 |
9 | BAA01g22060 | A01 | 11001799 | C | T | synonymous_variant | LOW | c.1089C>T|p.Leu363Leu |
S167 |
10 | BAA01g22060 | A01 | 11002923 | G | A | missense_variant | MODERATE | c.1645G>A|p.Asp549Asn |
S172 S217 |
11 | BAA01g22060 | A01 | 11003417 | C | T | missense_variant | MODERATE | c.1963C>T|p.Arg655Trp |
S237 |