Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21210 | A01 | 10486555 | G | A | missense_variant | MODERATE | c.860C>T|p.Ser287Leu |
S306 S308 |
2 | BAA01g21210 | A01 | 10487137 | G | A | missense_variant | MODERATE | c.365C>T|p.Ala122Val |
S287 |
3 | BAA01g21210 | A01 | 10487683 | C | T | upstream_gene_variant | MODIFIER | c.-5G>A| |
S4 |
4 | BAA01g21210 | A01 | 10487711 | C | T | upstream_gene_variant | MODIFIER | c.-33G>A| |
S176 |
5 | BAA01g21210 | A01 | 10488135 | C | T | upstream_gene_variant | MODIFIER | c.-457G>A| |
S201 |
6 | BAA01g21210 | A01 | 10488708 | C | T | upstream_gene_variant | MODIFIER | c.-1030G>A| |
S256 S39 |
7 | BAA01g21210 | A01 | 10488749 | G | A | upstream_gene_variant | MODIFIER | c.-1071C>T| |
S265 |
8 | BAA01g21210 | A01 | 10490426 | G | A | upstream_gene_variant | MODIFIER | c.-2748C>T| |
S236 |
9 | BAA01g21210 | A01 | 10490492 | A | G | upstream_gene_variant | MODIFIER | c.-2814T>C| |
S95 |
10 | BAA01g21210 | A01 | 10490726 | G | A | upstream_gene_variant | MODIFIER | c.-3048C>T| |
S134 S179 S193 |
11 | BAA01g21210 | A01 | 10490751 | G | A | upstream_gene_variant | MODIFIER | c.-3073C>T| |
S240 |
12 | BAA01g21210 | A01 | 10492177 | G | A | upstream_gene_variant | MODIFIER | c.-4499C>T| |
S95 |