Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39970 | A01 | 26541724 | C | T | synonymous_variant | LOW | c.2001G>A|p.Leu667Leu |
S46 |
2 | BAA01g39970 | A01 | 26542018 | G | A | synonymous_variant | LOW | c.1779C>T|p.Tyr593Tyr |
S149 |
3 | BAA01g39970 | A01 | 26542775 | C | A | missense_variant | MODERATE | c.1243G>T|p.Ala415Ser |
S282 |
4 | BAA01g39970 | A01 | 26542794 | G | A | synonymous_variant | LOW | c.1224C>T|p.Phe408Phe |
S298 |
5 | BAA01g39970 | A01 | 26543266 | G | A | missense_variant | MODERATE | c.752C>T|p.Pro251Leu |
S249 |
6 | BAA01g39970 | A01 | 26543718 | C | T | missense_variant | MODERATE | c.395G>A|p.Cys132Tyr |
S139 |
7 | BAA01g39970 | A01 | 26544212 | C | T | missense_variant | MODERATE | c.56G>A|p.Gly19Glu |
S56 |
8 | BAA01g39970 | A01 | 26544434 | G | A | upstream_gene_variant | MODIFIER | c.-167C>T| |
S66 |
9 | BAA01g39970 | A01 | 26544704 | C | T | upstream_gene_variant | MODIFIER | c.-437G>A| |
S73 S91 |
10 | BAA01g39970 | A01 | 26545217 | G | A | upstream_gene_variant | MODIFIER | c.-950C>T| |
S195 |
11 | BAA01g39970 | A01 | 26545647 | C | T | upstream_gene_variant | MODIFIER | c.-1380G>A| |
S180 |
12 | BAA01g39970 | A01 | 26546319 | C | T | upstream_gene_variant | MODIFIER | c.-2052G>A| |
S302 |
13 | BAA01g39970 | A01 | 26546569 | C | T | upstream_gene_variant | MODIFIER | c.-2302G>A| |
S148 S30 S31 |
14 | BAA01g39970 | A01 | 26546573 | C | T | upstream_gene_variant | MODIFIER | c.-2306G>A| |
S240 |
15 | BAA01g39970 | A01 | 26546976 | C | T | upstream_gene_variant | MODIFIER | c.-2709G>A| |
S293 |
16 | BAA01g39970 | A01 | 26547400 | G | A | upstream_gene_variant | MODIFIER | c.-3133C>T| |
S173 |
17 | BAA01g39970 | A01 | 26547468 | C | T | upstream_gene_variant | MODIFIER | c.-3201G>A| |
S119 |