Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45950 | A01 | 30599550 | G | A | missense_variant | MODERATE | c.2993C>T|p.Pro998Leu |
S243 S299 |
2 | BAA01g45950 | A01 | 30600431 | C | T | synonymous_variant | LOW | c.2112G>A|p.Arg704Arg |
S46 |
3 | BAA01g45950 | A01 | 30600598 | G | A | missense_variant | MODERATE | c.1945C>T|p.Arg649Trp |
S17 S181 |
4 | BAA01g45950 | A01 | 30601406 | G | A | synonymous_variant | LOW | c.1137C>T|p.Pro379Pro |
S189 |
5 | BAA01g45950 | A01 | 30601966 | C | T | missense_variant | MODERATE | c.577G>A|p.Glu193Lys |
S275 |
6 | BAA01g45950 | A01 | 30602068 | C | T | missense_variant | MODERATE | c.475G>A|p.Gly159Arg |
S164 |
7 | BAA01g45950 | A01 | 30602085 | G | A | missense_variant | MODERATE | c.458C>T|p.Ala153Val |
S149 |
8 | BAA01g45950 | A01 | 30602548 | C | T | upstream_gene_variant | MODIFIER | c.-6G>A| |
S32 |
9 | BAA01g45950 | A01 | 30603028 | C | T | upstream_gene_variant | MODIFIER | c.-486G>A| |
S177 |
10 | BAA01g45950 | A01 | 30603159 | C | T | upstream_gene_variant | MODIFIER | c.-617G>A| |
S72 S78 |
11 | BAA01g45950 | A01 | 30606009 | G | A | upstream_gene_variant | MODIFIER | c.-3467C>T| |
S86 |